PDB ID |
Authors |
First Page |
Medline Link |
Journal Name |
Title |
Volume No |
Publication Year |
|
|
|
|
|
|
|
|
1A0J |
H.K.Schroder, N.P.Willassen, A.O.Smalas |
780 |
9757092 |
Acta Crystallogr D Biol Crystallogr |
Structure of a non-psychrophilic trypsin from a cold-adapted fish species. |
54 |
1998 |
1A0L |
P.J.Pereira, A.Bergner, S.Macedo-Ribeiro, R.Huber, G.Matschiner, H.Fritz, C.P.Sommerhoff, W.Bode |
306 |
9521329 |
Nature |
Human beta-tryptase is a ring-like tetramer with active sites facing a central pore. |
392 |
1998 |
1A1Q |
R.A.Love, H.E.Parge, J.A.Wickersham, Z.Hostomsky, N.Habuka, E.W.Moomaw, T.Adachi, Z.Hostomska |
331 |
8861916 |
Cell |
The crystal structure of hepatitis C virus NS3 proteinase reveals a trypsin-like fold and a structural zinc binding site. |
87 |
1996 |
1A2C |
J.L.R.Steiner, M.Murakami, A.Tulinsky |
597 |
( 1A2C ) |
J Am Chem Soc |
Structure of thrombin inhibited by aeruginosin 298-A from a blue-green alga. |
120 |
1998 |
1A5H |
M.Renatus, W.Bode, R.Huber, J.Sturzebecher, D.Prasa, S.Fischer, U.Kohnert, M.T.Stubbs |
21713 |
9268299 |
J Biol Chem |
Structural mapping of the active site specificity determinants of human tissue-type plasminogen activator. Implications for the design of low molecular weight substrates and inhibitors. |
272 |
1997 |
1A5I |
M.Renatus, M.T.Stubbs, R.Huber, P.Bringmann, P.Donner, W.D.Schleuning, W.Bode |
13483 |
9354616 |
Biochemistry |
Catalytic domain structure of vampire bat plasminogen activator: a molecular paradigm for proteolysis without activation cleavage. |
36 |
1997 |
1AAL |
C.Eigenbrot, M.Randal, A.A.Kossiakoff |
75 |
1384034 |
Proteins |
Structural effects induced by mutagenesis affected by crystal packing factors: the structure of a 30-51 disulfide mutant of basic pancreatic trypsin inhibitor. |
14 |
1992 |
1AAP |
T.R.Hynes, M.Randal, L.A.Kennedy, C.Eigenbrot, A.A.Kossiakoff |
10018 |
2125487 |
Biochemistry |
X-ray crystal structure of the protease inhibitor domain of Alzheimer's amyloid beta-protein precursor. |
29 |
1990 |
1AB9 |
N.H.Yennawar, H.P.Yennawar, G.K.Farber |
7326 |
8003497 |
Biochemistry |
X-ray crystal structure of gamma-chymotrypsin in hexane. |
33 |
1994 |
1ABI |
X.Qiu, K.P.Padmanabhan, V.E.Carperos, A.Tulinsky, T.Kline, J.M.Maraganore, .2.Fenton 2d |
11689 |
1445905 |
Biochemistry |
Structure of the hirulog 3-thrombin complex and nature of the S' subsites of substrates and inhibitors. |
31 |
1992 |
1ABJ |
X.Qiu, K.P.Padmanabhan, V.E.Carperos, A.Tulinsky, T.Kline, J.M.Maraganore, .2.Fenton 2d |
11689 |
1445905 |
Biochemistry |
Structure of the hirulog 3-thrombin complex and nature of the S' subsites of substrates and inhibitors. |
31 |
1992 |
1ACB |
F.Frigerio, A.Coda, L.Pugliese, C.Lionetti, E.Menegatti, G.Amiconi, H.P.Schnebli, P.Ascenzi, M.Bolognesi |
107 |
1583684 |
J Mol Biol |
Crystal and molecular structure of the bovine alpha-chymotrypsin-eglin c complex at 2.0 A resolution. |
225 |
1992 |
1ADZ |
M.J.Burgering, L.P.Orbons, A.van der Doelen, J.Mulders, H.J.Theunissen, P.D.Grootenhuis, W.Bode, R.Huber, M.T.Stubbs |
395 |
9199408 |
J Mol Biol |
The second Kunitz domain of human tissue factor pathway inhibitor: cloning, structure determination and interaction with factor Xa. |
269 |
1997 |
1AE8 |
G.De Simone, G.Balliano, P.Milla, C.Gallina, C.Giordano, C.Tarricone, M.Rizzi, M.Bolognesi, P.Ascenzi |
558 |
9217260 |
J Mol Biol |
Human alpha-thrombin inhibition by the highly selective compounds N-ethoxycarbonyl-D-Phe-Pro-alpha-azaLys p-nitrophenyl ester and N-carbobenzoxy-Pro-alpha-azaLys p-nitrophenyl ester: a kinetic, thermodynamic and X-ray crystallographic study. |
269 |
1997 |
1AFE |
G.De Simone, G.Balliano, P.Milla, C.Gallina, C.Giordano, C.Tarricone, M.Rizzi, M.Bolognesi, P.Ascenzi |
558 |
9217260 |
J Mol Biol |
Human alpha-thrombin inhibition by the highly selective compounds N-ethoxycarbonyl-D-Phe-Pro-alpha-azaLys p-nitrophenyl ester and N-carbobenzoxy-Pro-alpha-azaLys p-nitrophenyl ester: a kinetic, thermodynamic and X-ray crystallographic study. |
269 |
1997 |
1AFQ |
N.H.Yennawar, H.P.Yennawar, G.K.Farber |
7326 |
8003497 |
Biochemistry |
X-ray crystal structure of gamma-chymotrypsin in hexane. |
33 |
1994 |
1AHT |
Z.Chen, Y.Li, A.M.Mulichak, S.D.Lewis, J.A.Shafer |
198 |
7574675 |
Arch Biochem Biophys |
Crystal structure of human alpha-thrombin complexed with hirugen and p-amidinophenylpyruvate at 1.6 A resolution. |
322 |
1995 |
1AKS |
A.Johnson, S.Krishnaswamy, P.V.Sundaram, V.Pattabhi |
311 |
( 1AKS ) |
Acta Crystallogr D Biol Crystallogr |
The first structure at 1.8 angstrom resolution of an active autolysate form of porcine alpha-trypsin. |
53 |
1997 |
1AMB |
J.Talafous, K.J.Marcinowski, G.Klopman, M.G.Zagorski |
7788 |
7516706 |
Biochemistry |
Solution structure of residues 1-28 of the amyloid beta-peptide. |
33 |
1994 |
1AMC |
J.Talafous, K.J.Marcinowski, G.Klopman, M.G.Zagorski |
7788 |
7516706 |
Biochemistry |
Solution structure of residues 1-28 of the amyloid beta-peptide. |
33 |
1994 |
1AMH |
J.J.Perona, C.S.Craik |
337 |
7795518 |
Protein Sci |
Structural basis of substrate specificity in the serine proteases. |
4 |
1995 |
1AN1 |
S.Di Marco, J.P.Priestle |
1465 |
9384562 |
Structure |
Structure of the complex of leech-derived tryptase inhibitor (LDTI) with trypsin and modeling of the LDTI-tryptase system. |
5 |
1997 |
1ANB |
M.E.McGrath, J.R.Vasquez, C.S.Craik, A.S.Yang, B.Honig, R.J.Fletterick |
3059 |
1554694 |
Biochemistry |
Perturbing the polar environment of Asp102 in trypsin: consequences of replacing conserved Ser214. |
31 |
1992 |
1ANC |
M.E.McGrath, J.R.Vasquez, C.S.Craik, A.S.Yang, B.Honig, R.J.Fletterick |
3059 |
1554694 |
Biochemistry |
Perturbing the polar environment of Asp102 in trypsin: consequences of replacing conserved Ser214. |
31 |
1992 |
1AND |
M.E.McGrath, B.L.Haymore, N.L.Summers, C.S.Craik, R.J.Fletterick |
1914 |
8448149 |
Biochemistry |
Structure of an engineered, metal-actuated switch in trypsin. |
32 |
1993 |
1ANE |
n/a |
n/a |
( 1ANE ) |
n/a |
n/a |
n/a |
n/a |
1AO5 |
D.E.Timm |
1418 |
9232643 |
Protein Sci |
The crystal structure of the mouse glandular kallikrein-13 (prorenin converting enzyme). |
6 |
1997 |
1AQ7 |
B.Sandler, M.Murakami, J.Clardy |
595 |
( 1AQ7 ) |
J Am Chem Soc |
Atomic structure of the trypsin-aeruginosin 98-B complex. |
120 |
1998 |
1AS4 |
C.M.Lukacs, H.Rubin, D.W.Christianson |
3297 |
9521649 |
Biochemistry |
Engineering an anion-binding cavity in antichymotrypsin modulates the "spring-loaded" serpin-protease interaction. |
37 |
1998 |
1ATA |
B.L.Grasberger, G.M.Clore, A.M.Gronenborn |
669 |
7922043 |
Structure |
High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site. |
2 |
1994 |
1ATB |
B.L.Grasberger, G.M.Clore, A.M.Gronenborn |
669 |
7922043 |
Structure |
High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site. |
2 |
1994 |
1ATD |
B.L.Grasberger, G.M.Clore, A.M.Gronenborn |
669 |
7922043 |
Structure |
High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site. |
2 |
1994 |
1ATE |
B.L.Grasberger, G.M.Clore, A.M.Gronenborn |
669 |
7922043 |
Structure |
High-resolution structure of Ascaris trypsin inhibitor in solution: direct evidence for a pH-induced conformational transition in the reactive site. |
2 |
1994 |
1ATT |
L.Mourey, J.P.Samama, M.Delarue, M.Petitou, J.Choay, D.Moras |
223 |
8331659 |
J Mol Biol |
Crystal structure of cleaved bovine antithrombin III at 3.2 A resolution. |
232 |
1993 |
1ATU |
S.E.Ryu, H.J.Choi, K.S.Kwon, K.N.Lee, M.H.Yu |
1181 |
8939743 |
Structure |
The native strains in the hydrophobic core and flexible reactive loop of a serine protease inhibitor: crystal structure of an uncleaved alpha1-antitrypsin at 2.7 A. |
4 |
1996 |
1AUJ |
S.L.Lee, R.S.Alexander, A.Smallwood, R.Trievel, L.Mersinger, P.C.Weber, C.Kettner |
13180 |
9341205 |
Biochemistry |
New inhibitors of thrombin and other trypsin-like proteases: hydrogen bonding of an aromatic cyano group with a backbone amide of the P1 binding site replaces binding of a basic side chain. |
36 |
1997 |
1AUT |
T.Mather, V.Oganessyan, P.Hof, R.Huber, S.Foundling, C.Esmon, W.Bode |
6822 |
9003757 |
EMBO J |
The 2.8 A crystal structure of Gla-domainless activated protein C. |
15 |
1996 |
1AV7 |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
1AVT |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
1AVU |
H.K.Song, S.W.Suh |
347 |
9466914 |
J Mol Biol |
Kunitz-type soybean trypsin inhibitor revisited: refined structure of its complex with porcine trypsin reveals an insight into the interaction between a homologous inhibitor from Erythrina caffra and tissue-type plasminogen activator. |
275 |
1998 |
1AVW |
H.K.Song, S.W.Suh |
347 |
9466914 |
J Mol Biol |
Kunitz-type soybean trypsin inhibitor revisited: refined structure of its complex with porcine trypsin reveals an insight into the interaction between a homologous inhibitor from Erythrina caffra and tissue-type plasminogen activator. |
275 |
1998 |
1AVX |
H.K.Song, S.W.Suh |
347 |
9466914 |
J Mol Biol |
Kunitz-type soybean trypsin inhibitor revisited: refined structure of its complex with porcine trypsin reveals an insight into the interaction between a homologous inhibitor from Erythrina caffra and tissue-type plasminogen activator. |
275 |
1998 |
1AWF |
M.P.Weir, S.S.Bethell, A.Cleasby, C.J.Campbell, R.J.Dennis, C.J.Dix, H.Finch, H.Jhoti, C.J.Mooney, S.Patel, C.M.Tang, M.Ward, A.J.Wonacott, C.W.Wharton |
6645 |
9578548 |
Biochemistry |
Novel natural product 5,5-trans-lactone inhibitors of human alpha- thrombin: mechanism of action and structural studies. |
37 |
1998 |
1AWH |
M.P.Weir, S.S.Bethell, A.Cleasby, C.J.Campbell, R.J.Dennis, C.J.Dix, H.Finch, H.Jhoti, C.J.Mooney, S.Patel, C.M.Tang, M.Ward, A.J.Wonacott, C.W.Wharton |
6645 |
9578548 |
Biochemistry |
Novel natural product 5,5-trans-lactone inhibitors of human alpha- thrombin: mechanism of action and structural studies. |
37 |
1998 |
1AXJ |
E.Liepinsh, M.Kitamura, T.Murakami, T.Nakaya, G.Otting |
975 |
9406543 |
Nat Struct Biol |
Pathway of chymotrypsin evolution suggested by the structure of the FMN-binding protein from Desulfovibrio vulgaris. |
4 |
1997 |
1AZ8 |
R.Alexander, T.Maduskuie, K.Mcnamara, A.Smallwood, A.Wei, P.Stouten |
n/a |
( 1AZ8 ) |
To be Published |
Unexpected Binding Mode of a Bis-Phenylamidine Factor Xa Inhibitor Complexed to Bovine Trypsin |
n/a |
n/a |
1AZZ |
J.J.Perona, C.A.Tsu, C.S.Craik, R.J.Fletterick |
5381 |
9154920 |
Biochemistry |
Crystal structure of an ecotin-collagenase complex suggests a model for recognition and cleavage of the collagen triple helix. |
36 |
1997 |
1B0C |
C.Hamiaux, J.Perez, T.Prange, S.Veesler, M.Ries-Kautt, P.Vachette |
697 |
( 1B0C ) |
J.Mol.Biol. |
The Bpti Decamer Observed in Acidic Ph Crystal Forms Pre-Exists as a Stable Species in Solution |
297 |
2000 |
1B1U |
S.Gourinath, A.Srinivasan, T.P.Singh |
287 |
( 1B1U ) |
Acta Crystallogr., Sect.D |
Structure of the Bifunctional Inhibitor of Trypsin and Alpha-Amylase from Ragi Seeds at 2.2 Angstrom Resolution |
55 |
2000 |
1BA7 |
P.De Meester, P.Brick, L.F.Lloyd, D.M.Blow, S.Onesti |
589 |
9761854 |
Acta Crystallogr D Biol Crystallogr |
Structure of the Kunitz-type soybean trypsin inhibitor (STI): implication for the interactions between members of the STI family and tissue-plasminogen activator. |
54 |
1998 |
1BA8 |
R.Krishnan, E.Zhang, K.Hakansson, R.K.Arni, A.Tulinsky, M.S.Lim-Wilby, O.E.Levy, J.E.Semple, T.K.Brunck |
12094 |
9724521 |
Biochemistry |
Highly selective mechanism-based thrombin inhibitors: structures of thrombin and trypsin inhibited with rigid peptidyl aldehydes. |
37 |
1998 |
1BB0 |
R.Krishnan, E.Zhang, K.Hakansson, R.K.Arni, A.Tulinsky, M.S.Lim-Wilby, O.E.Levy, J.E.Semple, T.K.Brunck |
12094 |
9724521 |
Biochemistry |
Highly selective mechanism-based thrombin inhibitors: structures of thrombin and trypsin inhibited with rigid peptidyl aldehydes. |
37 |
1998 |
1BBI |
M.H.Werner, D.E.Wemmer |
999 |
1734975 |
Biochemistry |
Three-dimensional structure of soybean trypsin/chymotrypsin Bowman-Birk inhibitor in solution. |
31 |
1992 |
1BBR |
P.D.Martin, W.Robertson, D.Turk, R.Huber, W.Bode, B.F.Edwards |
7911 |
1560020 |
J Biol Chem |
The structure of residues 7-16 of the A alpha-chain of human fibrinogen bound to bovine thrombin at 2.3-A resolution. |
267 |
1992 |
1BCU |
E.Conti, C.Rivetti, A.Wonacott, P.Brick |
229 |
9559654 |
FEBS Lett |
X-ray and spectrophotometric studies of the binding of proflavin to the S1 specificity pocket of human alpha-thrombin. |
425 |
1998 |
1BDA |
M.Renatus, R.A.Engh, M.T.Stubbs, R.Huber, S.Fischer, U.Kohnert, W.Bode |
4797 |
9305622 |
EMBO J |
Lysine 156 promotes the anomalous proenzyme activity of tPA: X-ray crystal structure of single-chain human tPA. |
16 |
1997 |
1BEF |
H.M.Murthy, S.Clum, R.Padmanabhan |
5573 |
10026173 |
J Biol Chem |
Dengue virus NS3 serine protease. Crystal structure and insights into interaction of the active site with substrates by molecular modeling and structural analysis of mutational effects. |
274 |
1999 |
1BG3 |
A.M.Mulichak, J.E.Wilson, K.Padmanabhan, R.M.Garavito |
555 |
9665168 |
Nat Struct Biol |
The structure of mammalian hexokinase-1. |
5 |
1998 |
1BHC |
C.Hamiaux, T.Prange, M.Ries-Kautt, A.Ducruix, S.Lafont, J.P.Astier, S.Veesler |
103 |
10089400 |
Acta Crystallogr D Biol Crystallogr |
The decameric structure of bovine pancreatic trypsin inhibitor (BPTI) crystallized from thiocyanate at 2.7 A resolution. |
55 |
1999 |
1BHX |
J.Wagner, J.Kallen, C.Ehrhardt, J.P.Evenou, D.Wagner |
3664 |
9733491 |
J Med Chem |
Rational design, synthesis, and X-ray structure of selective noncovalent thrombin inhibitors. |
41 |
1998 |
1BIK |
Y.Xu, P.D.Carr, J.M.Guss, D.L.Ollis |
955 |
9566199 |
J Mol Biol |
The crystal structure of bikunin from the inter-alpha-inhibitor complex: a serine protease inhibitor with two Kunitz domains. |
276 |
1998 |
1BIO |
H.Jing, Y.S.Babu, D.Moore, J.M.Kilpatrick, X.Y.Liu, J.E.Volanakis, S.V.Narayana |
1061 |
( 1BIO ) |
J.Mol.Biol. |
Structures of Native and Complexed Complement Factor D: Implications of the Atypical His57 Conformation and Self-Inhibitory Loop in the Regulation of Specific Serine Protease Activity |
282 |
1998 |
1BIP |
S.Strobl, P.Muhlhahn, R.Bernstein, R.Wiltscheck, K.Maskos, M.Wunderlich, R.Huber, R.Glockshuber, T.A.Holak |
8281 |
7599120 |
Biochemistry |
Determination of the three-dimensional structure of the bifunctional alpha-amylase/trypsin inhibitor from ragi seeds by NMR spectroscopy. |
34 |
1995 |
1BIT |
G.I.Berglund, A.O.Smalas, A.Hordvik |
725 |
( 1BIT ) |
Acta Crystallogr D Biol Crystallogr |
STRUCTURE OF ANIONIC SALMON TRYPSIN IN A 2ND CRYSTAL FORM. |
51 |
1995 |
1BJU |
S.Presnell, G.Patil, J.Conley, C.Mura, K.Jude, J.Bertrand, J.Powers, L.Williams |
n/a |
( 1BJU ) |
To be Published |
Structure and Mechanism of Sulfate Ion Mediated Inhibition of Serine Proteases |
n/a |
n/a |
1BJV |
S.R.Presnell, G.Patil, C.Mura, K.Jude, J.Conley, J.A.Bertrand, C.-M.Kam, J.C.Powers, L.D.Williams |
n/a |
( 1BJV ) |
To be Published |
Structure and Mechanism of Sulfate Ion Mediated Inhibition of Serine Proteases |
n/a |
n/a |
1BMA |
E.Peisach, D.Casebier, S.L.Gallion, P.Furth, G.A.Petsko, J.C.Hogan Jr., D.Ringe |
66 |
7604279 |
Science |
Interaction of a peptidomimetic aminimide inhibitor with elastase. |
269 |
1995 |
1BMM |
M.F.Malley, L.Tabernero, C.Y.Chang, S.L.Ohringer, D.G.Roberts, J.Das, J.S.Sack |
221 |
8745399 |
Protein Sci |
Crystallographic determination of the structures of human alpha-thrombin complexed with BMS-186282 and BMS-189090. |
5 |
1996 |
1BMN |
M.F.Malley, L.Tabernero, C.Y.Chang, S.L.Ohringer, D.G.Roberts, J.Das, J.S.Sack |
221 |
8745399 |
Protein Sci |
Crystallographic determination of the structures of human alpha-thrombin complexed with BMS-186282 and BMS-189090. |
5 |
1996 |
1BOQ |
R.J.Peters, A.K.Shiau, J.L.Sohl, D.E.Anderson, G.Tang, J.L.Silen, D.A.Agard |
12058 |
9724517 |
Biochemistry |
Pro region C-terminus:protease active site interactions are critical in catalyzing the folding of alpha-lytic protease. |
37 |
1998 |
1BPI |
S.Parkin, B.Rupp, H.Hope |
18 |
( 1BPI ) |
Acta Crystallogr D Biol Crystallogr |
Structure of bovine pancreatic trypsin inhibitor at 125 K: Definition of carboxyl-terminal residues Gly57 and Ala58. |
52 |
1996 |
1BPT |
A.T.Danishefsky, D.Housset, K.S.Kim, F.Tao, J.Fuchs, C.Woodward, A.Wlodawer |
577 |
8518731 |
Protein Sci |
Crevice-forming mutants in the rigid core of bovine pancreatic trypsin inhibitor: crystal structures of F22A, Y23A, N43G, and F45A. |
2 |
1993 |
1BRA |
J.J.Perona, C.A.Tsu, M.E.McGrath, C.S.Craik, R.J.Fletterick |
934 |
8478942 |
J Mol Biol |
Relocating a negative charge in the binding pocket of trypsin. |
230 |
1993 |
1BRB |
J.J.Perona, C.A.Tsu, C.S.Craik, R.J.Fletterick |
919 |
7683059 |
J Mol Biol |
Crystal structures of rat anionic trypsin complexed with the protein inhibitors APPI and BPTI. |
230 |
1993 |
1BRC |
J.J.Perona, C.A.Tsu, M.E.McGrath, C.S.Craik, R.J.Fletterick |
934 |
8478942 |
J Mol Biol |
Relocating a negative charge in the binding pocket of trypsin. |
230 |
1993 |
1BT7 |
G.Barbato, D.O.Cicero, M.C.Nardi, C.Steinkuhler, R.Cortese, R.De Francesco, R.Bazzo |
370 |
( 1BT7 ) |
J.Mol.Biol. |
The Solution Structure of the N-Terminal Proteinase Domain of the Hepatitis C Virus (Hcv) Ns3 Protein Provides New Insights Into its Activation and Catalytic Mechanism |
289 |
1999 |
1BTH |
A.van de Locht, W.Bode, R.Huber, B.F.Le Bonniec, S.R.Stone, C.T.Esmon, M.T.Stubbs |
2977 |
9214615 |
EMBO J |
The thrombin E192Q-BPTI complex reveals gross structural rearrangements: implications for the interaction with antithrombin and thrombomodulin. |
16 |
1997 |
1BTI |
A.T.Danishefsky, D.Housset, K.S.Kim, F.Tao, J.Fuchs, C.Woodward, A.Wlodawer |
577 |
8518731 |
Protein Sci |
Crevice-forming mutants in the rigid core of bovine pancreatic trypsin inhibitor: crystal structures of F22A, Y23A, N43G, and F45A. |
2 |
1993 |
1BTP |
Y.Odagaki, H.Nakai, K.Senokuchi, M.Kawamura, N.Hamanaka, M.Nakamura, K.Tomoo, T.Ishida |
12849 |
7548040 |
Biochemistry |
Unique binding of a novel synthetic inhibitor, N-[3-[4-[4-(amidinophenoxy)carbonyl]phenyl]-2-methyl-2-propenoyl]- N-allylglycine methanesulfonate, to bovine trypsin, revealed by the crystal structure of the complex. |
34 |
1995 |
1BTW |
B.A.Katz, J.Finermoore, R.Mortezaei, D.H.Rich, R.M.Stroud |
8264 |
( 1BTW ) |
Biochemistry |
EPISELECTION - NOVEL K-I-SIMILAR-TO NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE. |
34 |
1995 |
1BTX |
B.A.Katz, J.Finer-Moore, R.Mortezaei, D.H.Rich, R.M.Stroud |
8264 |
7599119 |
Biochemistry |
Episelection: novel Ki approximately nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface. |
34 |
1995 |
1BTY |
B.A.Katz, J.Finer-Moore, R.Mortezaei, D.H.Rich, R.M.Stroud |
8264 |
7599119 |
Biochemistry |
Episelection: novel Ki approximately nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface. |
34 |
1995 |
1BTZ |
B.A.Katz, J.Finer-Moore, R.Mortezaei, D.H.Rich, R.M.Stroud |
8264 |
7599119 |
Biochemistry |
Episelection: novel Ki approximately nanomolar inhibitors of serine proteases selected by binding or chemistry on an enzyme surface. |
34 |
1995 |
1BXJ |
I.Zhukov, L.Jaroszewski, A.Bierzynski |
n/a |
( 1BXJ ) |
To be Published |
The Conservative Mutation met-->Leu Effects Folding and Stability of Squash Trypsin Inhibitor Cmti-I |
n/a |
n/a |
1BZ5 |
C.Hamiaux, J.Perez, T.Prange, S.Veesler, M.Ries-Kautt, P.Vachette |
697 |
( 1BZ5 ) |
J.Mol.Biol. |
The Bpti Decamer Observed in Acidic Ph Crystal Forms Pre-Exists as a Stable Species in Solution |
297 |
2000 |
1BZX |
R.Helland, I.Leiros, G.I.Berglund, N.P.Willassen, A.O.Smalas |
317 |
9760170 |
Eur J Biochem |
The crystal structure of anionic salmon trypsin in complex with bovine pancreatic trypsin inhibitor. |
256 |
1998 |
1C1N |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1N ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1O |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1O ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1P |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1P ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1Q |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1Q ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1R |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1R ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1S |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1S ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C1T |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C1T ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2A |
H.K.Song, Y.S.Kim, J.K.Yang, J.Moon, J.Y.Lee, S.W.Suh |
1133 |
( 1C2A ) |
J.Mol.Biol. |
Crystal Structure of a 16 kDa Double-Headed Bowman-Birk Trypsin Inhibitor from Barley Seeds at 1.9 A Resolution |
293 |
1999 |
1C2D |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2D ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2E |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2E ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2F |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2F ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2G |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2G ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2H |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2H ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2I |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2I ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2J |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2J ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2K |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2K ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2L |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2L ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C2M |
B.A.Katz, J.M.Clark, J.S.Finer-Moore, T.E.Jenkins, C.R.Johnson, M.J.Ross, C.Luong, W.R.Moore, R.M.Stroud |
608 |
( 1C2M ) |
Nature |
Design of Potent Selective Zinc-Mediated Serine Protease Inhibitors |
391 |
1998 |
1C5L |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5L ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5M |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5M ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5N |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5N ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5O |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5O ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5P |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5P ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5Q |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5Q ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5R |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5R ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5S |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5S ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5T |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5T ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5U |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5U ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5V |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5V ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5W |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5W ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5X |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5X ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase Type Plasminogen Activator |
7 |
2000 |
1C5Y |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5Y ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C5Z |
B.A.Katz, R.Mackman, C.Luong, K.Radika, A.Martelli, P.A.Sprengeler, J.Wang, H.Chan, L.Wong |
299 |
( 1C5Z ) |
Chem.Biol. |
Structural Basis for Selectivity of a Small Molecule, S1-Binding, Submicromolar Inhibitor of Urokinase-Type Plasminogen Activator |
7 |
2000 |
1C9P |
U.Rester, W Bode, M.Moser, M.A.Parry, R.Huber, E.Auerswald |
93 |
( 1C9P ) |
J.Mol.Biol. |
Structure of the Complex of the Antistasin-Type Inhibitor Bdellastasin with Trypsin and Modelling of the Bdellastasin-Microplasmin System |
293 |
1999 |
1C9T |
U.Rester, W.Bode, M.Moser, M.A.Parry, R.Huber, E.Auerswald |
93 |
( 1C9T ) |
J.Mol.Biol. |
Structure of the Complex of the Antistasin-Type Inhibitor Bdellastasin with Trypsin and Modelling of the Bdellastasin-Microplasmin System |
293 |
1999 |
1CA0 |
A.J.Scheidig, T.R.Hynes, L.A.Pelletier, J.A.Wells, A.A.Kossiakoff |
1806 |
9300481 |
Protein Sci |
Crystal structures of bovine chymotrypsin and trypsin complexed to the inhibitor domain of Alzheimer's amyloid beta-protein precursor (APPI) and basic pancreatic trypsin inhibitor (BPTI): engineering of inhibitors with altered specificities. |
6 |
1997 |
1CA8 |
R.Krishnan, E.Zhang, K.Hakansson, R.K.Arni, A.Tulinsky, M.S.Lim-Wilby, O.E.Levy, J.E.Semple, T.K.Brunck |
12094 |
9724521 |
Biochemistry |
Highly selective mechanism-based thrombin inhibitors: structures of thrombin and trypsin inhibited with rigid peptidyl aldehydes. |
37 |
1998 |
1CAU |
T.-P.Ko, J.D.Ng, J.Day, A.Greenwood, A.McPherson |
n/a |
( 1CAU ) |
To be Published |
Determination of Three Crystal Structures of Canavalin by Molecular Replacement |
n/a |
n/a |
1CAV |
T.P.Ko, J.D.Ng, A.McPherson |
729 |
8310056 |
Plant Physiol |
The three-dimensional structure of canavalin from jack bean (Canavalia ensiformis). |
101 |
1993 |
1CAW |
T.-P.Ko, J.D.Ng, J.Day, A.Greenwood, A.McPherson |
n/a |
( 1CAW ) |
To be Published |
Determination of Three Crystal Structures of Canavalin by Molecular Replacement |
n/a |
n/a |
1CAX |
T.-P.Ko, J.D.Ng, J.Day, A.Greenwood, A.McPherson |
n/a |
( 1CAX ) |
To be Published |
Determination of Three Crystal Structures of Canavalin by Molecular Replacement |
n/a |
n/a |
1CBW |
A.J.Scheidig, T.R.Hynes, L.A.Pelletier, J.A.Wells, A.A.Kossiakoff |
1806 |
9300481 |
Protein Sci |
Crystal structures of bovine chymotrypsin and trypsin complexed to the inhibitor domain of Alzheimer's amyloid beta-protein precursor (APPI) and basic pancreatic trypsin inhibitor (BPTI): engineering of inhibitors with altered specificities. |
6 |
1997 |
1CCV |
J.Bania, D.Stachowiak, A.Polanowski |
680 |
( 1CCV ) |
Eur J Biochem |
Primary structure and properties of the cathepsin G chymotrypsin inhibitor from the larval hemolymph of Apis mellifera. |
262 |
1999 |
1CE5 |
N.Ota, C.Stroupe, J.M.S.Ferreira-Da-Silva, S.S.Shah, M.Mares-Guia, A.T.Brunger |
641 |
( 1CE5 ) |
Proteins: Struct., Funct., Genet. |
Non-Boltzmann Thermodynamic Integration (Nbti) for Macromolecular Systems: Relative Free Energy of Binding of Trypsin to Benzamidine and Benzylamine |
37 |
1999 |
1CGI |
H.J.Hecht, M.Szardenings, J.Collins, D.Schomburg |
711 |
1870127 |
J Mol Biol |
Three-dimensional structure of the complexes between bovine chymotrypsinogen A and two recombinant variants of human pancreatic secretory trypsin inhibitor (Kazal-type). |
220 |
1991 |
1CGJ |
H.J.Hecht, M.Szardenings, J.Collins, D.Schomburg |
711 |
1870127 |
J Mol Biol |
Three-dimensional structure of the complexes between bovine chymotrypsinogen A and two recombinant variants of human pancreatic secretory trypsin inhibitor (Kazal-type). |
220 |
1991 |
1CHG |
S.T.Freer, J.Kraut, J.D.Robertus, H.T.Wright, N.H.Xuong |
1997 |
5442169 |
Biochemistry |
Chymotrypsinogen: 2.5-angstrom crystal structure, comparison with alpha-chymotrypsin, and implications for zymogen activation. |
9 |
1970 |
1CHO |
M.Fujinaga, A.R.Sielecki, R.J.Read, W.Ardelt, M.Laskowski Jr., M.N.James |
397 |
3477645 |
J Mol Biol |
Crystal and molecular structures of the complex of alpha-chymotrypsin with its inhibitor turkey ovomucoid third domain at 1.8 A resolution. |
195 |
1987 |
1CIQ |
J.L.Neira, B.Davis, A.G.Ladurner, A.M.Buckle, P.Gay G de, A.R.Fersht |
189 |
9079381 |
Fold Des |
Towards the complete structural characterization of a protein folding pathway: the structures of the denatured, transition and native states for the association/folding of two complementary fragments of cleaved chymotrypsin inhibitor 2. Direct evidence for a nucleation-condensation mechanism. |
1 |
1996 |
1CIR |
J.L.Neira, B.Davis, A.G.Ladurner, A.M.Buckle, P.Gay G de, A.R.Fersht |
189 |
9079381 |
Fold Des |
Towards the complete structural characterization of a protein folding pathway: the structures of the denatured, transition and native states for the association/folding of two complementary fragments of cleaved chymotrypsin inhibitor 2. Direct evidence for a nucleation-condensation mechanism. |
1 |
1996 |
1CIS |
P.Osmark, P.Sorensen, F.M.Poulsen |
11007 |
8218165 |
Biochemistry |
Context dependence of protein secondary structure formation: the three-dimensional structure and stability of a hybrid between chymotrypsin inhibitor 2 and helix E from subtilisin Carlsberg. |
32 |
1993 |
1CJK |
J.J.G.Tesmer, R.K.Sunahara, R.A.Johnson, G.Gosselin, A.G.Gilman, S.R.Sprang |
756 |
( 1CJK ) |
Science |
Two Metal Ion Catalysis in Adenylyl Cyclase Revealed by its Complexes with ATP Analogs, Mg2+, Mn2+, and Zn2+ |
285 |
1999 |
1CJT |
J.J.G.Tesmer, R.K.Sunahara, R.A.Johnson, G.Gosselin, A.G.Gilman, S.R.Sprang |
756 |
( 1CJT ) |
Science |
Two Metal Ion Catalysis in Adenylyl Cyclase Revealed by its Complexes with ATP Analogs, Mg2+, Mn2+, and Zn2+ |
285 |
1999 |
1CJU |
J.J.G.Tesmer, R.K.Sunahara, R.A.Johnson, G.Gosselin, A.G.Gilman, S.R.Sprang |
756 |
( 1CJU ) |
Science |
Two Metal Ion Catalysis in Adenylyl Cyclase Revealed by its Complexes with ATP Analogs, Mg2+, Mn2+, and Zn2+ |
285 |
1999 |
1CJV |
J.J.G.Tesmer, R.K.Sunahara, R.A.Johnson, G.Gosselin, A.G.Gilman, S.R.Sprang |
756 |
( 1CJV ) |
Science |
Two Metal Ion Catalysis in Adenylyl Cyclase Revealed by its Complexes with ATP Analogs, Mg2+, Mn2+, and Zn2+ |
285 |
1999 |
1CO7 |
G.F.Stamper, D.Ringe, L.Hedstrom |
n/a |
( 1CO7 ) |
Unpublished |
R117H Mutant Structure of Trypsin/Bpti Inhibitor Complex |
n/a |
n/a |
1COA |
S.E.Jackson, M.Moracci, N.elMasry, C.M.Johnson, A.R.Fersht |
11259 |
8218191 |
Biochemistry |
Effect of cavity-creating mutations in the hydrophobic core of chymotrypsin inhibitor 2. |
32 |
1993 |
1CPX |
J.T.Bukrinsky, M.J.Bjerrum, A.Kadziola |
16555 |
9843422 |
Biochemistry |
Native carboxypeptidase A in a new crystal environment reveals a different conformation of the important tyrosine 248. |
37 |
1998 |
1CQ4 |
Y.W.Chen, K.Stott, M.F.Perutz |
1257 |
9990011 |
Proc Natl Acad Sci U S A |
Crystal structure of a dimeric chymotrypsin inhibitor 2 mutant containing an inserted glutamine repeat. |
96 |
1999 |
1CTI |
T.A.Holak, D.Gondol, J.Otlewski, T.Wilusz |
635 |
2614837 |
J Mol Biol |
Determination of the complete three-dimensional structure of the trypsin inhibitor from squash seeds in aqueous solution by nuclear magnetic resonance and a combination of distance geometry and dynamical simulated annealing. |
210 |
1989 |
1D0D |
R.St.Charles, K.Padmanabhan, R.V.Arni, K.P.Padmanabhan, A.Tulinsky |
265 |
( 1D0D ) |
Protein Sci. |
Structure of Tick Anticoagulant Peptide at 1.6 A Resolution Complexed with Bovine Pancreatic Trypsin Inhibitor |
9 |
2000 |
1D5S |
M.A.Dunstone, W.Dai, J.C.Whisstock, J.Rossjohn, R.N.Pike, S.C.Feil, B.F.Le Bonniec, M.W.Parker, S.P.Bottomley |
417 |
( 1D5S ) |
Protein Sci. |
Cleaved Antitrypsin Polymers at Atomic Resolution |
9 |
2000 |
1D6R |
J.Koepke, U.Ermler, E.Warkentin, G.Wenzl, P.Flecker |
477 |
( 1D6R ) |
J.Mol.Biol. |
Crystal Structure of Cancer Chemopreventive Bowman-Birk Inhibitor in Ternary Complex with Bovine Trypsin at 2.3 A Resolution. Structural Basis of Janus- Faced Serine Protease Inhibitor Specificity |
298 |
2000 |
1DE7 |
C.Sadasivan, V.C.Yee |
36942 |
( 1DE7 ) |
J.Biol.Chem. |
Interaction of the Factor Xiii Activation Peptide with Alpha-Thrombin. Crystal Structure of its Enzyme-Substrate Analog Complex |
275 |
2000 |
1DEE |
M.Graille, E.A.Stura, A.L.Corper, B.J.Sutton, M.J.Taussig, J.B.Charbonnier, G.J.Silverman |
5399 |
( 1DEE ) |
Proc.Nat.Acad.Sci.USA |
Crystal Structure of a Staphylococcus Aureus Protein a Domain Complexed with the Fab Fragment of a Human Igm Antibody: Structural Basis for Recognition of B-Cell Receptors and Superantigen Activity |
97 |
2000 |
1DF9 |
H.M.Krishna Murthy, K.Judge, L.Delucas, R.Padmanabhan |
759 |
( 1DF9 ) |
J.Mol.Biol. |
Crystal Structure of Dengue Virus Ns3 Protease in Complex with a Bowman-Birk Inhibitor: Implications for Drug Design. |
301 |
2000 |
1DG1 |
K.Abel, M.Yoder, R.Hilgenfeld, F.Jurnak |
1153 |
( 1DG1 ) |
Structure (London) |
An Alpha to Beta Conformational Switch in EF-TU |
4 |
1996 |
1DGR |
T.-P.Ko, A.McPherson |
n/a |
( 1DGR ) |
To be Published |
Structures of the Rhombohedral and Orthorhombic Crystals of Canavalin from Jack Bean |
n/a |
n/a |
1DGW |
T.-P.Ko, A.McPherson |
n/a |
( 1DGW ) |
To be Published |
Structures of the Rhombohedral and Orthorhombic Crystals of Canavalin from Jack Bean |
n/a |
n/a |
1DIT |
R.Krishnan, A.Tulinsky, G.P.Vlasuk, D.Pearson, P.Vallar, P.Bergum, T.K.Brunck, W.C.Ripka |
422 |
8868478 |
Protein Sci |
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R.Friedrich, W.Bode |
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1EB1 |
R.Friedrich, T.Steinmetzer, W.Bode |
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Crystal Structure of Thrombin-Jt54 |
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J.W.Liebeschuetz, S.D.Jones, P.J.Morgan, C.W.Murray, A.D.Rimmer, J.M.E.Roscoe, B.Waszkowycz, P.M.Welsh, W.A.Wylie, S.C.Young, H.Martin, J.Mahler, L.Brady' K.Wilkinson |
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Pro_Select: Combining Structure-Based Drug Design and Array-Based Chemistry for Rapid Lead Discovery. 2. The Development of a Series of Highly Potent and Selective Factor Xa Inhibitors |
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1F0S |
S.Maignan, J.P.Guilloteau, S.Pouzieux, Y.M.Choi-Sledeski, M.R.Becker, S.I.Klein, W.R.Ewing, H.W.Pauls, A.P.Spada, V.Mikol |
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1F1R |
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Structure of Homoprotocatechuate 2,3-Dioxygenase from Arthrobacter Globiformis Cm-2 : A Manganese Dependent Extradiol Dioxygenase |
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1F1U |
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Structure of Homoprotocatechuate 2,3-Dioxygenase from Arthrobacter Globiformis Cm-2 : A Manganese Dependent Extradiol Dioxygenase |
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1F1V |
M.W.Vetting, J.D.Lipscomb, L.P.Wackett, L.Que Jr, D.H.Ohlendorf |
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Structure of Homoprotocatechuate 2,3-Dioxygenase from Arthrobacter Globiformis Cm-2 : A Manganese Dependent Extradiol Dioxygenase |
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1F1X |
M.W.Vetting, J.D.Lipscomb, L.P.Wackett, L.Que Jr, D.H.Ohlendorf |
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Crystal Structure of Homoprotocatechuate 2,3-Dioxygenase from Brevibacterium Fuscum |
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H.Nar, M.Bauer, A.Schmid, J.Stassen, W.Wienen, H.W.Priepke, I.K.Kauffmann, U.J.Ries, N.H.Hauel |
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H.Nar, M.Bauer, A.Schmid, J.Stassen, W.Wienen, H.W.Priepke, I.K.Kauffmann, U.J.Ries, N.H.Hauel |
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2000 |
1G3C |
E.Toyota, K.K.S.Ng, H.Sekizaki, K.Itoh, K.Tanizawa, M.N.G.James |
471 |
( 1G3C ) |
J.Mol.Biol. |
X-Ray Crystallographic Analyses of Complexes between Bovine Beta-Trypsin and Schiff Base Copper(II) or Iron(III) Chelates |
305 |
2000 |
1G3D |
E.Toyota, K.K.S.Ng, H.Sekizaki, K.Itoh, K.Tanizawa, M.N.G.James |
471 |
( 1G3D ) |
J.Mol.Biol. |
X-Ray Crystallographic Analyses of Complexes between Bovine Beta-Trypsin and Schiff Base Copper(II) or Iron(III) Chelates |
305 |
2000 |
1G3E |
E.Toyota, K.K.S.Ng, H.Sekizaki, K.Itoh, K.Tanizawa, M.N.G.James |
471 |
( 1G3E ) |
J.Mol.Biol. |
X-Ray Crystallographic Analyses of Complexes between Bovine Beta-Trypsin and Schiff Base Copper(II) or Iron(III) Chelates |
305 |
2000 |
1G6X |
A.Addlagatta, H.Czapinska, J.Otlewski, S.Krzywda, M.Jaskolski |
649 |
( 1G6X ) |
Acta Crystallogr., Sect.D |
Ultrahigh-Resolution Structure of a Bpti Mutant |
57 |
2001 |
1G9I |
G.Zhu, Q.Huang, Y.Zhu, Y.Li, C.Chi, Y.Tang |
98 |
( 1G9I ) |
Biochim.Biophys.Acta |
X-Ray Studies on an Artificial Mung Bean Inhibitor Complex with Bovine Beta-Trypsin in Neat Cyclohexane |
1546 |
2001 |
1GBA |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBB |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBC |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBD |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBE |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBF |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBH |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBI |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBJ |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBK |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBL |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBM |
J.E.Mace, D.A.Agard |
720 |
7500345 |
J Mol Biol |
Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. |
254 |
1995 |
1GBT |
W.F.Mangel, P.T.Singer, D.M.Cyr, T.C.Umland, D.L.Toledo, R.M.Stroud, J.W.Pflugrath, R.M.Sweet |
8351 |
2252895 |
Biochemistry |
Structure of an acyl-enzyme intermediate during catalysis: (guanidinobenzoyl)trypsin. |
29 |
1990 |
1GCD |
M.Harel, C.T.Su, F.Frolow, Y.Ashani, I.Silman, J.L.Sussman |
909 |
1942036 |
J Mol Biol |
Refined crystal structures of "aged" and "non-aged" organophosphoryl conjugates of gamma-chymotrypsin. |
221 |
1991 |
1GCT |
M.M.Dixon, B.W.Matthews |
7033 |
2819046 |
Biochemistry |
Is gamma-chymotrypsin a tetrapeptide acyl-enzyme adduct of alpha-chymotrypsin? |
28 |
1989 |
1GDN |
W.R.Rypniewski, P.Oestergaard, M.Noerregaard-Madsen, M.Dauter, K.S.Wilson |
8 |
( 1GDN ) |
Acta Crystallogr., Sect.D |
Fusarium Oxysporum Trypsin at Atomic Resolution at 100 and 283 K: A Study of Ligand Binding |
57 |
2001 |
1GDQ |
W.R.Rypniewski, P.Oestergaard, M.Noerregaard-Madsen, M.Dauter, K.S.Wilson |
8 |
( 1GDQ ) |
Acta Crystallogr., Sect.D |
Fusarium Oxysporum Trypsin at Atomic Resolution at 100 and 283 K: A Study of Ligand Binding |
57 |
2001 |
1GDU |
W.R.Rypniewski, P.Oestergaard, M.Noerregaard-Madsen, M.Dauter, K.S.Wilson |
8 |
( 1GDU ) |
Acta Crystallogr., Sect.D |
Fusarium Oxysporum Trypsin at Atomic Resolution at 100 and 283 K: A Study of Ligand Binding |
57 |
2001 |
1GFC |
D.Kohda, H.Terasawa, S.Ichikawa, K.Ogura, H.Hatanaka, V.Mandiyan, A.Ullrich, J.Schlessinger, F.Inagaki |
1029 |
7881903 |
Structure |
Solution structure and ligand-binding site of the carboxy-terminal SH3 domain of GRB2. |
2 |
1994 |
1GFD |
D.Kohda, H.Terasawa, S.Ichikawa, K.Ogura, H.Hatanaka, V.Mandiyan, A.Ullrich, J.Schlessinger, F.Inagaki |
1029 |
7881903 |
Structure |
Solution structure and ligand-binding site of the carboxy-terminal SH3 domain of GRB2. |
2 |
1994 |
1GG6 |
D.J.Neidhart, Y.Wei, C.Cassidy, J.Lim, W.C.Cleland, P.A.Frey |
n/a |
( 1GG6 ) |
To be Published |
Crystal Stucture of Gamma Chymotrypsin with N-Acetyl-Phenylalanine Trifluoromethyl Ketone Bound at the Active Site |
n/a |
n/a |
1GGD |
D.J.Neidhart, Y.Wei, C.Cassidy, J.Lim, W.C.Cleland, P.A.Frey |
n/a |
( 1GGD ) |
To be Published |
Crystal Stucture of Gamma Chymotrypsin with N-Acetyl-Phenylalanine Trifluoromethyl Ketone Bound at the Active Site |
n/a |
n/a |
1GHA |
H.P.Yennawar, N.H.Yennawar, G.K.Farber |
577 |
( 1GHA ) |
J Am Chem Soc |
A STRUCTURAL EXPLANATION FOR ENZYME MEMORY IN NONAQUEOUS SOLVENTS. |
117 |
1995 |
1GHB |
H.P.Yennawar, N.H.Yennawar, G.K.Farber |
577 |
( 1GHB ) |
J Am Chem Soc |
A STRUCTURAL EXPLANATION FOR ENZYME MEMORY IN NONAQUEOUS SOLVENTS. |
117 |
1995 |
1GHV |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GHV ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GHW |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GHW ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GHX |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GHX ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GHY |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GHY ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GHZ |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GHZ ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI0 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI0 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI1 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI1 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI2 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI2 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI3 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI3 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI4 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI4 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI5 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI5 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI6 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI6 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI7 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI7 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI8 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI8 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GI9 |
B.A.Katz, K.Elrod, C.Luong, M.Rice, R.L.Mackman, P.A.Sprengeler, J.Spencer, J.Hatayte, J.Janc, J.Link, J.Litvak, R.Rai, K.Rice, S.Sideris, E.Verner, W.Young |
1451 |
( 1GI9 ) |
J.Mol.Biol. |
A Novel Serine Protease Inhibition Motif Involving a Multi-Centered Short Hydrogen Bonding Network at the Active Site |
307 |
2001 |
1GJ4 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ4 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJ5 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ5 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJ6 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ6 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJ7 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ7 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJ8 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ8 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJ9 |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJ9 ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJA |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJA ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJB |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJB ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJC |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJC ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GJD |
B.A.Katz, P.A.Sprengeler, C.Luong, E.Verner, K.Elrod, M.Kirtley, J.Janc, J.R.Spencer, J.G.Breitenbucher, H.Hui, D.Mcgee, D.Allen, A.Martelli, R.L.Mackman |
1107 |
( 1GJD ) |
Chem.Biol. |
Engineering Inhibitors Highly Selective for the S1 Sites of Ser190 Trypsin-Like Serine Protease Drug Targets |
8 |
2002 |
1GL0 |
A.Roussel, M.Mathieu, A.Dobbs, B.Luu, C.Cambillau, C.Kellenberger |
38893 |
( 1GL0 ) |
J.Biol.Chem. |
Complexation of Two Proteic Insect Inhibitors to the Active Site of Chymotrypsin Suggests Decoupled Roles for Binding and Selectivity |
276 |
2001 |
1GL1 |
A.Roussel, M.Mathieu, A.Dobbs, B.Luu, C.Cambillau, C.Kellenberger |
38893 |
( 1GL1 ) |
J.Biol.Chem. |
Complexation of Two Proteic Insect Inhibitors to the Active Site of Chymotrypsin Suggests Decoupled Roles for Binding and Selectivity |
276 |
2001 |
1GM2 |
A.B.E.Brauer, G.Kelly, S.J.Matthews, R.J.Leatherbarrow |
59 |
( 1GM2 ) |
J.Biomol.Struct.Dyn. |
The 1H-NMR Solution Structure of the Antitryptic Core Peptide of Bowman-Birk Inhibitor Proteins: A Minimal Canonical Loop |
20 |
2002 |
1GMC |
N.H.Yennawar, H.P.Yennawar, G.K.Farber |
7326 |
8003497 |
Biochemistry |
X-ray crystal structure of gamma-chymotrypsin in hexane. |
33 |
1994 |
1GMD |
N.H.Yennawar, H.P.Yennawar, G.K.Farber |
7326 |
8003497 |
Biochemistry |
X-ray crystal structure of gamma-chymotrypsin in hexane. |
33 |
1994 |
1GMH |
M.Harel, C.T.Su, F.Frolow, Y.Ashani, I.Silman, J.L.Sussman |
909 |
1942036 |
J Mol Biol |
Refined crystal structures of "aged" and "non-aged" organophosphoryl conjugates of gamma-chymotrypsin. |
221 |
1991 |
1GNA |
N.J.Skelton, K.C.Garcia, D.V.Goeddel, C.Quan, J.P.Burnier |
13581 |
7947768 |
Biochemistry |
Determination of the solution structure of the peptide hormone guanylin: observation of a novel form of topological stereoisomerism. |
33 |
1994 |
1GNB |
N.J.Skelton, K.C.Garcia, D.V.Goeddel, C.Quan, J.P.Burnier |
13581 |
7947768 |
Biochemistry |
Determination of the solution structure of the peptide hormone guanylin: observation of a novel form of topological stereoisomerism. |
33 |
1994 |
1GNS |
O.Almog, D.T.Gallagher, J.E.Ladner, S.Strausberg, P.Alexander, P.Bryan, G.L.Gilliland |
n/a |
( 1GNS ) |
To be Published |
Structural Basis of Thermostability: Analysis of Stabilizing Mutations in Calcium Independent Subtilisin Bpn' |
n/a |
n/a |
1GNV |
O.Almog, D.T.Gallagher, J.E.Ladner, S.Strausberg, P.Alexander, P.Bryan, G.L.Gilliland |
n/a |
( 1GNV ) |
To be Published |
Structural Basis of Thermostability: Analysis of Stabilizing Mutations in Calcium-Independent Subtilisin |
n/a |
n/a |
1GNX |
A.Guasch, M.Vallmitjana, R.Perez, E.Querol, J.A.Perez-Pons, M.Coll |
n/a |
( 1GNX ) |
To be Published |
Beta-Glucosidase from Streptomyces |
n/a |
n/a |
1GON |
A.Guasch, M.Vallmitjana, R.Perez, E.Querol, J.A.Perez-Pons, M.Coll |
n/a |
( 1GON ) |
To be Published |
Crystal Structure of a Family 1 Beta-Glucosidase from Streptomyces |
n/a |
n/a |
1H2A |
Y.Higuchi, T.Yagi, N.Yasuoka |
1671 |
9438867 |
Structure |
Unusual ligand structure in Ni-Fe active center and an additional Mg site in hydrogenase revealed by high resolution X-ray structure analysis. |
5 |
1997 |
1H2R |
Y.Higuchi, H.Ogata, K.Miki, N.Yasuoka, T.Yagi |
549 |
( 1H2R ) |
Structure (London) |
Removal of the Bridging Ligand Atom at the Ni-Fe Active Site of [Nife] Hydrogenase Upon Reduction with H2, as Revealed by X-Ray Structure Analysis at 1.4 A Resolution |
7 |
1999 |
1H34 |
J.Debreczeni, G.Bunkoczi, B.Girmann, G.Sheldrick |
393 |
( 1H34 ) |
Acta Crystallogr.,Sect.D |
In-House Phase Determination of the Lima Bean Trypsin Inhibitor: A Low-Resolution Sulfur-Sad Case |
59 |
2003 |
1H4W |
G.Katona, G.I.Berglund, J.Hajdu, L.Graf, L.Szilagyi |
1209 |
( 1H4W ) |
J.Mol.Biol. |
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M.J.Van Raaij, G.Schoehn, M.R.Burda, S.Miller |
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E.Skordalakes, G.G.Dodson, D.S.Green, C.A.Goodwin, M.F.Scully, H.R.Hudson, V.V.Kakkar, J.J.Deadman |
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E.Skordalakes, G.G.Dodson, D.S.Green, C.A.Goodwin, M.F.Scully, H.R.Hudson, V.V.Kakkar, J.J.Deadman |
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J.H.Cho, S.Jeon Chung, N.-C.Ha, S.Yun, M.S.Han, H.Cheon Lee, D.H.Kim, K.Y.Choi, B.-H.Oh |
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Crystal Structure of Bovine Pancreatic Carboxypeptidase a Complexed with D-N-Hydroxyaminocarbonyl Phenylalanine at 2.3A |
n/a |
n/a |
1HDT |
L.Tabernero, C.Y.Chang, S.L.Ohringer, W.F.Lau, E.J.Iwanowicz, W.C.Han, T.C.Wang, S.M.Seiler, D.G.Roberts, J.S.Sack |
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Crystal Structure of Bovine Pancreatic |
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1HEE |
J.H.Cho, S.Jeon Chung, N.-C.Ha, S.Yun, M.S.Han, H.Cheon Lee, D.H.Kim, K.Y.Choi, B.-H.Oh |
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Crystal Structure of Bovine Pancreatic Carboxypeptidase a Complexed with L-N-Hydroxyaminocarbonyl Phenylalanine at 2.3 A |
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1HFD |
H.Jing, Y.S.Babu, D.Moore, J.M.Kilpatrick, X.Y.Liu, J.E.Volanakis, S.V.Narayana |
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1HJA |
J.Ding, M.A.Qasim, M.Laskowski Junior, M.N.G.James |
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Crystal Structure of Lys18 Variant of Turkey Ovomucoid Inhibitor Third Domain Complexed with Alpha-Chymotrypsin at 2.3 A |
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n/a |
1HKO |
F.W.Muskett, D.Whitford |
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Cytochrome B5NMR Structure of Bovine |
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1HLT |
I.I.Mathews, K.P.Padmanabhan, A.Tulinksy, J.E.Sadler |
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A.Jasanoff, G.Wagner, D.C.Wiley |
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J.A.Cuesta-Seijo, S.Garcia-Granda |
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Crystal Structure of Trypsin at Atomic Resolution Using Data from Laboratory Source |
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1JBL |
M.L.J.Korsinczky, H.J.Schirra, K.J.Rosengren, J.West, B.A.Condie, L.Otvos, M.A.Anderson, D.J.Craik |
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311 |
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M.L.J.Korsinczky, H.J.Schirra, K.J.Rosengren, J.West, B.A.Condie, L.Otvos, M.A.Anderson, D.J.Craik |
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C.Eigenbrot, D.Kirchhofer, M.S.Dennis, L.Santell, R.A.Lazarus, J.Stamos, M.H.Ultsch |
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9 |
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C.Chen, C.H.Hsu, N.Y.Su, Y.C.Lin, S.H.Chiou, S.H.Wu |
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276 |
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1JIR |
G.Wu, G.Zhu, Q.Huang, M.Qian, Y.Tang |
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Crystal Structure of Beta-Trypsin Complex with Amylamine in Cyclohexane |
n/a |
n/a |
1JJO |
C.Briand, S.V.Kozlov, P.Sonderegger, M.G.Gruetter |
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Crystal Structure of Neuroserpin: A Neuronal Serpin Involved in a Conformational Disease. |
505 |
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I.V.Kurinov, R.W.Harrison |
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8845765 |
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I.V.Kurinov, R.W.Harrison |
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J.L.Battiste, R.Li, C.Woodward |
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1JV9 |
J.L.Battiste, R.Li, C.Woodward |
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Betacore, a Designed Water Soluble Four-Stranded Antiparallel B-Sheet Protein |
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1K1M |
F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
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J.Mol.Biol. |
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F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
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F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
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J.Mol.Biol. |
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313 |
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1K1P |
F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
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J.Mol.Biol. |
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313 |
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1K21 |
F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
593 |
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J.Mol.Biol. |
Factorising Ligand Affinity: A Combined Thermodynamic and Crystallographic Study of Trypsin and Thrombin Inhibition |
313 |
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1K22 |
F.Dullweber, M.T.Stubbs, D.Musil, J.Sturzebecher, G.Klebe |
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Crystal Structure of the Bifunctional Soybean Bowman-Birk Inhibitor at 0.28 Nm Resolution. Structural Peculiarities in a Folded Protein Conformation |
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Biochemistry |
Crystal structure of phenylmethanesulfonyl fluoride-treated human chymase at 1.9 A. |
36 |
1997 |
1KSN |
K.R.Guertin, C.J.Gardner, S.I.Klein, A.L.Zulli, M.Czekaj, Y.Gong, A.P.Spada, D.L.Cheney, S.Maignan, J.-P.Guilloteau, K.D.Brown, D.C.Colussi, V.Chu, C.L.Heran, S.R.Morgan, R.G.Bentley, C.T.Dunwiddie, R.J.Leadley, H.W.Pauls |
1671 |
( 1KSN ) |
Bioorg.Med.Chem.Lett. |
Optimization of the Beta-Aminoester Class of Factor Xa Inhibitors. Part 2: Identification of Fxv673 as a Potent and Selective Inhibitor with Excellent in Vivo Anticoagulant Activity |
12 |
2002 |
1KXA |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KXB |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KXC |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KXD |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KXE |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KXF |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
1KY9 |
T.Krojer, M.Garrido-Franco, R.Huber, M.Ehrmann, T.Clausen |
455 |
( 1KY9 ) |
Nature |
Crystal Structure of Degp (Htra) Reveals a Novel Protease-Chaperone Machine |
416 |
2002 |
1L1N |
S.C.Mosimann, M.M.Chernaia, S.Sia, S.Plotch, M.N.G.James |
1032 |
( 1L1N ) |
J.Mol.Biol. |
Refined X-Ray Crystallographic Structure of the Poliovirus 3C Gene Product |
273 |
1997 |
1L2E |
M.J.Bernett, S.I.Blaber, I.A.Scarisbrick, P.Dhanarajan, S.M.Thompson, M.Blaber |
n/a |
( 1L2E ) |
To be Published |
Crystal Structure and Biochemical Characterization of Human Kallikrein 6 Reveals a Trypsin-Like Kallikrein is Expressed in the Central Nervous System |
n/a |
n/a |
1LCN |
C.Hamiaux, S.Lafont, M.Ries-Kautt, M.C.Vaney, A.Ducruix, T.Prange |
n/a |
( 1LCN ) |
To be Published |
Crystal Structure of Lysozyme Complexed with Thiocyanate at 1.6 Angstroms |
n/a |
n/a |
1LD5 |
T.Cierpicki, J.Otlewski |
647 |
( 1LD5 ) |
J.Mol.Biol. |
NMR Structures of Two Variants of Bovine Pancreatic Trypsin Inhibitor (Bpti) Reveal Unexpected Influence of Mutations on Protein Structure and Stability |
321 |
2002 |
1LD6 |
T.Cierpicki, J.Otlewski |
647 |
( 1LD6 ) |
J.Mol.Biol. |
NMR Structures of Two Variants of Bovine Pancreatic Trypsin Inhibitor (Bpti) Reveal Unexpected Influence of Mutations on Protein Structure and Stability |
321 |
2002 |
1LDT |
M.T.Stubbs, R.Morenweiser, J.Sturzebecher, M.Bauer, W.Bode, R.Huber, G.P.Piechottka, G.Matschiner, C.P.Sommerhoff, H.Fritz, E.A.Auerswald |
19931 |
9242660 |
J Biol Chem |
The three-dimensional structure of recombinant leech-derived tryptase inhibitor in complex with trypsin. Implications for the structure of human mast cell tryptase and its inhibition. |
272 |
1997 |
1LHC |
P.C.Weber, S.L.Lee, F.A.Lewandowski, M.C.Schadt, C.W.Chang, C.A.Kettner |
3750 |
7893672 |
Biochemistry |
Kinetic and crystallographic studies of thrombin with Ac-(D)Phe-Pro-boroArg-OH and its lysine, amidine, homolysine, and ornithine analogs. |
34 |
1995 |
1LHD |
P.C.Weber, S.L.Lee, F.A.Lewandowski, M.C.Schadt, C.W.Chang, C.A.Kettner |
3750 |
7893672 |
Biochemistry |
Kinetic and crystallographic studies of thrombin with Ac-(D)Phe-Pro-boroArg-OH and its lysine, amidine, homolysine, and ornithine analogs. |
34 |
1995 |
1LHE |
P.C.Weber, S.L.Lee, F.A.Lewandowski, M.C.Schadt, C.W.Chang, C.A.Kettner |
3750 |
7893672 |
Biochemistry |
Kinetic and crystallographic studies of thrombin with Ac-(D)Phe-Pro-boroArg-OH and its lysine, amidine, homolysine, and ornithine analogs. |
34 |
1995 |
1LHF |
P.C.Weber, S.L.Lee, F.A.Lewandowski, M.C.Schadt, C.W.Chang, C.A.Kettner |
3750 |
7893672 |
Biochemistry |
Kinetic and crystallographic studies of thrombin with Ac-(D)Phe-Pro-boroArg-OH and its lysine, amidine, homolysine, and ornithine analogs. |
34 |
1995 |
1LHG |
P.C.Weber, S.L.Lee, F.A.Lewandowski, M.C.Schadt, C.W.Chang, C.A.Kettner |
3750 |
7893672 |
Biochemistry |
Kinetic and crystallographic studies of thrombin with Ac-(D)Phe-Pro-boroArg-OH and its lysine, amidine, homolysine, and ornithine analogs. |
34 |
1995 |
1LKA |
M.S.Weiss, S.Panjikar, E.Nowak, P.A.Tucker |
1407 |
( 1LKA ) |
Acta Crystallogr., Sect.D |
Metal Binding to Porcine Pancreatic Elastase: Calcium or not Calcium |
58 |
2002 |
1LKB |
M.S.Weiss, S.Panjikar, E.Nowak, P.A.Tucker |
1407 |
( 1LKB ) |
Acta Crystallogr., Sect.D |
Metal Binding to Porcine Pancreatic Elastase: Calcium or not Calcium |
58 |
2002 |
1LMW |
G.Spraggon, C.Phillips, U.K.Nowak, C.P.Ponting, D.Saunders, C.M.Dobson, D.I.Stuart, E.Y.Jones |
681 |
8591045 |
Structure |
The crystal structure of the catalytic domain of human urokinase-type plasminogen activator. |
3 |
1995 |
1LO6 |
M.J.Bernett, S.I.Blaber, I.A.Scarisbrick, P.Dhanarajan, S.M.Thompson, M.Blaber |
n/a |
( 1LO6 ) |
To be Published |
Crystal Structure and Biochemical Characterization of Human Kallikrein 6 Reveals a Trypsin-Like Kallikrein is Expressed in the Central Nervous System |
n/a |
n/a |
1LPG |
H.Matter, E.Defossa, U.Heinelt, P.M.Blohm, D.Schneider, A.Mueller, S.Herok, H.Schreuder, A.Liesum, B.Brachvogel, P.Loenze, A.Walser, F.Al-Obeidi, P.Wildgoose |
2749 |
( 1LPG ) |
J.Med.Chem. |
Design and Quantitative Structure-Activity Relationship of 3-Amidinobenzyl-1H-Indole-2-Carboxyamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa. |
45 |
2002 |
1LPK |
H.Matter, E.Defossa, U.Heinelt, P.M.Blohm, D.Schneider, A.Mueller, S.Herok, H.A.Schreuder, A.Liesum, V.Brachvogel, P.Loenze, A.Walser, F.Al-Obeidi, P.Wildgoose |
2749 |
( 1LPK ) |
J.Med.Chem. |
Design and Quantitative Structure-Activity Relationship of 3-Amidinobenzyl-1H-Indole-2-Carboxamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa |
45 |
2002 |
1LPZ |
H.Matter, E.Defossa, U.Heinelt, P.M.Blohm, D.Schneider, A.Mueller, S.Herok, H.A.Schreuder, A.Liesum, V.Brachvogel, P.Loenze, A.Walser, F.Al-Obeidi, P.Wildgoose |
2749 |
( 1LPZ ) |
J.Biol.Chem. |
Design and Quantitative Structure-Activity Relationship of 3-Amidinobenzyl-1H-Indole-2-Carboxamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa |
45 |
2002 |
1LQ8 |
J.A.Huntington, M.Kjellberg, J.Stenflo |
205 |
( 1LQ8 ) |
Structure |
Crystal Structure of Protein C Inhibitor Provides Insights Into Hormone Binding and Heparin Activation |
11 |
2003 |
1LQD |
H.Matter, E.Defossa, U.Heinelt, P.M.Blohm, D.Schneider, A.Mueller, S.Herok, H.A.Schreuder, A.Liesum, V.Brachvogel, P.Loenze, A.Walser, F.Al-Obeidi, P.Wildgoose |
2749 |
( 1LQD ) |
J.Med.Chem. |
Design and Quantitative Structure-Activity Relationship of 3-Amidinobenzyl-1H-Indel-2-Carboxamides as Potent, Nonchiral, and Selective Inhibitors of Blood Coagulation Factor Xa |
45 |
2002 |
1LQE |
H.Matter, E.Defossa, U.Heinelt, P.M.Blohm, D.Schneider, A.Mueller, S.Herok, H.A.Schreuder, A.Liesum, V.Brachvogel, P.Loenze, A.Walser, F.Al-Obeidi, P.Wildgoose |
2749 |
( 1LQE ) |
J.Med.Chem. |
Design and Quantitative Structure-Activity Relationship of 3-Aminidobenzyl-1H-Indol-2-Carboxiamides as Potent, Non-Chrial, and Selective Inhibitors of Factor Xa |
45 |
2002 |
1LQX |
J.-H.Gan, J.Wu, Z.-Q.Wang, Y.-H.Wang, Z.-X.Huang, Z.-X.Xia |
1298 |
( 1LQX ) |
Acta Crystallogr., Sect.D |
Structures of V45E and V45Y Mutants and Structure Comparison of a Variety of Cytochrome B5 Mutants |
58 |
2002 |
1LR6 |
J.-H.Gan, J.Wu, Z.-Q.Wang, Y.-H.Wang, Z.-X.Huang, Z.-X.Xia |
1298 |
( 1LR6 ) |
Acta Crystallogr., Sect.D |
Structures of V45E and V45Y Mutants and Structure Comparison of a Variety of Cytochrome B5 Mutants |
58 |
2002 |
1LTB |
E.A.Merritt, S.E.Pronk, T.K.Sixma, K.H.Kalk, B.A.van Zanten, W.G.Hol |
88 |
8276119 |
FEBS Lett |
Structure of partially-activated E. coli heat-labile enterotoxin (LT) at 2.6 A resolution. |
337 |
1994 |
1LU0 |
R.Thaimattam, E.Tykarska, A.Bierzynski, G.M.Sheldrick, M.Jaskolski |
1448 |
( 1LU0 ) |
Acta Crystallogr., Sect.D |
Atomic Resolution Structure of Squash Trypsin Inhibitor: Unexpected Metal Coordination |
58 |
2002 |
1LVB |
J.Phan, A.Zdanov, A.G.Evdokimov, J.E.Tropea, H.K.Peters III, R.B.Kapust, M.Li, A.Wlodawer, D.S.Waugh |
n/a |
( 1LVB ) |
To be Published |
Structural Basis for the Substrate Specificity of Tobacco Etch Virus Protease |
n/a |
n/a |
1LVM |
J.Phan, A.Zdanov, A.G.Evdokimov, J.E.Tropea, H.K.Peters III, R.B.Kapust, M.Li, A.Wlodawer, D.S.Waugh |
n/a |
( 1LVM ) |
To be Published |
Structural Basis for the Substrate Specificity of Tobacco Etch Virus Protease |
n/a |
n/a |
1LVO |
K.Anand, G.J.Palm, J.R.Mesters, S.G.Siddell, J.Ziebuhr, R.Hilgenfeld |
3213 |
( 1LVO ) |
Embo J. |
Structure of Coronavirus Main Proteinase Reveals Combination of a Chymotrypsin Fold with an Extra Alpha-Helical Domain |
21 |
2002 |
1LVY |
M.Schiltz, W.Shepard, R.Fourme, T.Prange, E.DeLaFortelle, G.Bricogne |
78 |
( 1LVY ) |
Acta Crystallogr D Biol Crystallogr |
High-pressure krypton gas and statistical heavy-atom refinement: A successful combination of tools for macromolecular structure determination. |
53 |
1997 |
1LW6 |
E.S.Radisky, D.E.Koshland Jr. |
10316 |
( 1LW6 ) |
Proc.Nat.Acad.Sci.USA |
A Clogged Gutter Mechanism for Protease Inhibitors |
99 |
2002 |
1LZX |
H.Li, H.Shimizu, M.Flinspach, J.Jamal, W.Yang, M.Xian, T.Cai, E.Z.Wen, Q.Jia, P.G.Wang, T.L.Poulos |
13868 |
( 1LZX ) |
Biochemistry |
The Novel Binding Mode of N-Alkyl-N'-Hydroxyguanidine to Neuronal Nitric Oxide Synthase Provides Mechanistic Insights Into No Biosynthesis |
41 |
2002 |
1LZZ |
H.Li, H.Shimizu, M.Flinspach, J.Jamal, W.Yang, M.Xian, T.Cai, E.Z.Wen, Q.Jia, P.G.Wang, T.L.Poulos |
13868 |
( 1LZZ ) |
Biochemistry |
The Novel Binding Mode of N-Alkyl-N'-Hydroxyguanidine to Neuronal Nitric Oxide Synthase Provides Mechanistic Insights Into No Biosynthesis |
41 |
2002 |
1M00 |
H.Li, H.Shimizu, M.Flinspach, J.Jamal, W.Yang, M.Xian, T.Cai, E.Z.Wen, Q.Jia, P.G.Wang, T.L.Poulos |
13868 |
( 1M00 ) |
Biochemistry |
The Novel Binding Mode of N-Alkyl-N'-Hydroxyguanidine to Neuronal Nitric Oxide Synthase Provides Mechanistic Insights Into No Biosynthesis |
41 |
2002 |
1M20 |
P.Yao, J.Wu, Y.-H.Wang, B.-Y.Sun, Z.-X.Xia, Z.-X.Huang |
4287 |
( 1M20 ) |
Eur.J.Biochem. |
X-Ray Crystallography, Cd and Kinetic Studies Revealed the Essence of the Abnormal Behaviors of the Cytochrome B5 Phe35--> Try Mutant |
269 |
2002 |
1M2I |
J.Wu, Y.-H.Wang, J.-H.Gan, W.-H.Wang, B.-Y.Sun, Z.-X.Huang, Z.-X.Xia |
1225 |
( 1M2I ) |
Chin.J.Chem. |
Structures of Cytochrome B5 Mutated at the Charged Surface-Residues and Their Interactions with Cytochrome C |
20 |
2002 |
1M2M |
J.Wu, Y.-H.Wang, J.-H.Gan, W.-H.Wang, B.-Y.Sun, Z.-X.Huang, Z.-X.Xia |
1225 |
( 1M2M ) |
Chin.J.Chem. |
Structures of Cytochrome B5 Mutated at the Charged Surface-Residues and Their Interactions with Cytochrome C |
20 |
2002 |
1M59 |
Z.-Q.Wang, J.Wu, Y.-H.Wang, W.Qian, Y.Xie, Z.-X.Xia, Z.-X.Huang |
1212 |
( 1M59 ) |
Chin.J.Chem. |
Proline40 is Essential to Maintaining Cytochrome B5 Stability and its Electron Transfer with Cytochrome C |
20 |
2002 |
1M9U |
Y.Tang, D.Liang, T.Jiang, J.Zhang, L.Gui, W.Chang |
57 |
( 1M9U ) |
J.Mol.Biol. |
Crystal Structure of Earthworm Fibrinolytic Enzyme Component A: Revealing the Structural Determinants of its Dual Fibrinolytic Activity |
321 |
2002 |
1MAX |
J.A.Bertrand, J.Oleksyszyn, C.M.Kam, B.Boduszek, S.Presnell, R.R.Plaskon, F.L.Suddath, J.C.Powers, L.D.Williams |
3147 |
8605148 |
Biochemistry |
Inhibition of trypsin and thrombin by amino(4-amidinophenyl)methanephosphonate diphenyl ester derivatives: X-ray structures and molecular models. |
35 |
1996 |
1MAY |
J.A.Bertrand, J.Oleksyszyn, C.M.Kam, B.Boduszek, S.Presnell, R.R.Plaskon, F.L.Suddath, J.C.Powers, L.D.Williams |
3147 |
8605148 |
Biochemistry |
Inhibition of trypsin and thrombin by amino(4-amidinophenyl)methanephosphonate diphenyl ester derivatives: X-ray structures and molecular models. |
35 |
1996 |
1MBM |
I.H.Barrette-Ng, K.K.-S.Ng, B.L.Mark, D.Van Aken, M.M.Cherney, C.Garen, Y.Kolodenko, A.E.Gorbalenya, E.J.Snijder, M.N.G.James |
39960 |
( 1MBM ) |
J.Biol.Chem. |
Structure of Arterivirus Nsp4: The Smallest Chymotrypsin-Like Proteinase with an Alpha/Beta C-Terminal Extension and Alternate Conformations of the Oxyanion Hole |
277 |
2002 |
1MBQ |
E.Toyota, K.K.S.Ng, S.Kuninaga, H.Sekizaki, K.Itoh, K.Tanizawa, M.N.G.James |
391 |
( 1MBQ ) |
J.Mol.Biol. |
Crystal Structure and Nucleotide Sequence of an Anionic Trypsin from Chum Salmon (Oncorhynchus Keta) in Comparison with Atlantic Salmon (Salmo Salar) and Bovine Trypsin |
324 |
2002 |
1MCT |
Q.Huang, S.Liu, Y.Tang |
1022 |
8445634 |
J Mol Biol |
Refined 1.6 A resolution crystal structure of the complex formed between porcine beta-trypsin and MCTI-A, a trypsin inhibitor of the squash family. Detailed comparison with bovine beta-trypsin and its complex. |
229 |
1993 |
1MCV |
J.Ay, K.Hilpert, N.Krauss, J.Schneider-Mergener, W.Hoehne |
247 |
( 1MCV ) |
Acta Crystallogr., Sect.D |
Structure of a Hybrid Squash Inhibitor in Complex with Porcine Pancreatic Elastase at 1.8 A Resolution |
59 |
2003 |
1MIT |
J.Liu, O.Prakash, M.Cai, Y.Gong, Y.Huang, L.Wen, J.J.Wen, J.K.Huang, R.Krishnamoorthi |
1516 |
8634282 |
Biochemistry |
Solution structure and backbone dynamics of recombinant Cucurbita maxima trypsin inhibitor-V determined by NMR spectroscopy. |
35 |
1996 |
1MKW |
M.G.Malkowski, P.D.Martin, J.C.Guzik, B.F.Edwards |
1438 |
9232645 |
Protein Sci |
The co-crystal structure of unliganded bovine alpha-thrombin and prethrombin-2: movement of the Tyr-Pro-Pro-Trp segment and active site residues upon ligand binding. |
6 |
1997 |
1MKX |
M.G.Malkowski, P.D.Martin, J.C.Guzik, B.F.Edwards |
1438 |
9232645 |
Protein Sci |
The co-crystal structure of unliganded bovine alpha-thrombin and prethrombin-2: movement of the Tyr-Pro-Pro-Trp segment and active site residues upon ligand binding. |
6 |
1997 |
1MMJ |
T.Kinoshita, I.Nakanishi, A.Sato, T.Tada |
21 |
( 1MMJ ) |
Bioorg.Med.Chem.Lett. |
True Interaction Mode of Porcine Pancreatic Elastase with Fr136706, a Potent Peptidyl Inhibitor |
13 |
2003 |
1MMV |
L.E.Bretscher, H.Li, T.L.Poulos, O.W.Griffith |
n/a |
( 1MMV ) |
To be Published |
Structural Characterization and Kinetics of Nitric Oxide Synthase Inhibition by Novel N5-(Iminoalkyl)- and N5-(Iminoalkenyl)-Ornithines |
n/a |
2003 |
1MMW |
L.E.Bretscher, H.Li, T.L.Poulos, O.W.Griffith |
n/a |
( 1MMW ) |
To be Published |
Structural Characterization and Kinetics of Nitric Oxide Synthase Inhibition by Novel N5-(Iminoalkyl)- and N5-(Iminoalkenyl)-Ornithines |
n/a |
2003 |
1MSK |
M.M.Dixon, S.Huang, R.G.Matthews, M.Ludwig |
1263 |
8939751 |
Structure |
The structure of the C-terminal domain of methionine synthase: presenting S-adenosylmethionine for reductive methylation of B12. |
4 |
1996 |
1MTN |
C.Capasso, M.Rizzi, E.Menegatti, P.Ascenzi, M.Bolognesi |
26 |
9179777 |
J Mol Recognit |
Crystal structure of the bovine alpha-chymotrypsin:Kunitz inhibitor complex. An example of multiple protein:protein recognition sites. |
10 |
1997 |
1MTS |
M.T.Stubbs, R.Huber, W.Bode |
103 |
7498454 |
FEBS Lett |
Crystal structures of factor Xa specific inhibitors in complex with trypsin: structural grounds for inhibition of factor Xa and selectivity against thrombin. |
375 |
1995 |
1MTU |
M.T.Stubbs, R.Huber, W.Bode |
103 |
7498454 |
FEBS Lett |
Crystal structures of factor Xa specific inhibitors in complex with trypsin: structural grounds for inhibition of factor Xa and selectivity against thrombin. |
375 |
1995 |
1MTV |
M.T.Stubbs, R.Huber, W.Bode |
103 |
7498454 |
FEBS Lett |
Crystal structures of factor Xa specific inhibitors in complex with trypsin: structural grounds for inhibition of factor Xa and selectivity against thrombin. |
375 |
1995 |
1MTW |
M.T.Stubbs, R.Huber, W.Bode |
103 |
7498454 |
FEBS Lett |
Crystal structures of factor Xa specific inhibitors in complex with trypsin: structural grounds for inhibition of factor Xa and selectivity against thrombin. |
375 |
1995 |
1N6X |
R.B.G.Ravelli, H.K.Schroder Leiros, B.Pan, M.Caffrey, S.Mcsweeney |
217 |
( 1N6X ) |
Structure |
Specific Radiation-Damage Can be Used to Solve Macromolecular Crystal Structures |
11 |
2003 |
1N6Y |
R.B.G.Ravelli, H.K.Schroder Leiros, B.Pan, M.Caffrey, S.Mcsweeney |
217 |
( 1N6Y ) |
Structure |
Specific Radiation-Damage Can be Used to Solve Macromolecular Crystal Structures |
11 |
2003 |
1N7A |
R.B.G.Ravelli, H.K.Schroder Leiros, B.Pan, M.Caffrey, S.Mcsweeney |
217 |
( 1N7A ) |
Structure |
Specific Radiation-Damage Can be Used to Solve Macromolecular Crystal Structures |
11 |
2003 |
1N7B |
R.B.G.Ravelli, H.K.Schroder Leiros, B.Pan, M.Caffrey, S.Mcsweeney |
217 |
( 1N7B ) |
Structure |
Specific Radiation-Damage Can be Used to Solve Macromolecular Crystal Structures |
11 |
2003 |
1N8O |
C.Cambillau, S.Spinelli, M.Lauwereys |
n/a |
( 1N8O ) |
To be Published |
Crystal Structure of a Complex between Bovine Chymotrypsin and Ecotin at 2.0 A Resolution |
n/a |
n/a |
1NAG |
A.T.Danishefsky, D.Housset, K.S.Kim, F.Tao, J.Fuchs, C.Woodward, A.Wlodawer |
577 |
8518731 |
Protein Sci |
Crevice-forming mutants in the rigid core of bovine pancreatic trypsin inhibitor: crystal structures of F22A, Y23A, N43G, and F45A. |
2 |
1993 |
1NC6 |
M.J.Costanzo, S.C.Yabut, H.R.Almond Jr., P.Andrade-Gordon, T.W.Corcoran, L.De Garavilla, J.A.Kauffman, W.M.Abraham, R.Recacha, D.Chattopadhyay, B.E.Maryanoff |
3865 |
( 1NC6 ) |
J.Med.Chem. |
Potent, Small-Molecule Inhibitors of Human Mast Cell Tryptase. Antiasthmatic Action of a Dipeptide-Based Transition-State Analogue Containing a Benzothiazole Ketone. |
46 |
2003 |
1NES |
E.F.Meyer Jr., R.Radhakrishnan, G.M.Cole, L.G.Presta |
533 |
3640831 |
J Mol Biol |
Structure of the product complex of acetyl-Ala-Pro-Ala with porcine pancreatic elastase at 1.65 A resolution. |
189 |
1986 |
1NKX |
S.Sharma, J.Jasti, J.Kumar, A.K.Mohanty, T.P.Singh |
485 |
( 1NKX ) |
J.Mol.Biol. |
Crystal Structure of a Proteolytically Generated Functional Monoferric C-Lobe of Bovine Lactoferrin at 1.9A Resolution |
331 |
2003 |
1NN6 |
K.K.Reiling, J.Krucinski, L.J.Miercke, W.W.Raymond, G.H.Caughey, R.M.Stroud |
2616 |
( 1NN6 ) |
Biochemistry |
Structure of Human Pro-Chymase: A Model for the Activating Transition of Granule-Associated Proteases. |
42 |
2003 |
1NRN |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NRO |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NRP |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NRQ |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NRR |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NRS |
I.I.Mathews, K.P.Padmanabhan, V.Ganesh, A.Tulinsky, M.Ishii, J.Chen, C.W.Turck, S.R.Coughlin, .2.Fenton 2nd |
3266 |
8136362 |
Biochemistry |
Crystallographic structures of thrombin complexed with thrombin receptor peptides: existence of expected and novel binding modes. |
33 |
1994 |
1NTP |
A.A.Kossiakoff |
281 |
( 1NTP ) |
Basic Life Sci. |
Use of the Neutron Diffraction-H(Slash)D Exchange Technique to Determine the Conformational Dynamics of Trypsin |
27 |
1984 |
1O2G |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2G ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2H |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2H ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2I |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2I ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2J |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2J ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2K |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2K ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2L |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2L ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2M |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2M ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2N |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2N ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2O |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2O ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2P |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.-F.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2P ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors |
329 |
2003 |
1O2Q |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2Q ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2R |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2R ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2S |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2S ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2T |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2T ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2U |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2U ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2V |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2V ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2W |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2W ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2X |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2X ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2Y |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2Y ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O2Z |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O2Z ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O30 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O30 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O31 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O31 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O32 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O32 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O33 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O33 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O34 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O34 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O35 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O35 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O36 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O36 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O37 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O37 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O38 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O38 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O39 |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O39 ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3A |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3A ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3B |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3B ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3C |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3C ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3D |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3D ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3E |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3E ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3F |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3F ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3G |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3G ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3H |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3H ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3I |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3I ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3J |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3J ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3K |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
( 1O3K ) |
J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3L |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
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J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3M |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
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J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3N |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
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J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3O |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
93 |
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J.Mol.Biol. |
Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-Directed Serine Protease Inhibitors. |
329 |
2003 |
1O3P |
B.A.Katz, K.Elrod, E.Verner, R.L.Mackman, C.Luong, W.D.Shrader, M.Sendzik, J.R.Spencer, P.A.Sprengeler, A.Kolesnikov, V.W.Tai, H.C.Hui, J.G.Breitenbucher, D.Allen, J.W.Janc |
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J.Mol.Biol. |
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1O8Y |
U.Marx, M.Korsinczky, H.Schirra, A.Jones, B.Condie, L.Otvos, D.Craik |
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J.Biol.Chem. |
Enzymatic Cyclization of a Potent Bowman-Birk Protease Inhibitor, Sunflower Trypsin Inhibitor-1, and Solution Structure of an Acyclic Precursor Peptide |
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U.Marx, M.Korsinczky, H.Schirra, A.Jones, B.Condie, L.Otvos, D.Craik |
21782 |
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J.Biol.Chem. |
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Protein Sci. |
The Solution Structure of Bovine Pancreatic Trypsin Inhibitor at High Pressure |
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1OA6 |
M.P.Williamson, K.Akasaka, M.Refaee |
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Protein Sci. |
The Solution Structure of Bovine Pancreatic Trypsin Inhibitor at High Pressure |
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1OIS |
N.Lue, A.Sharma, A.Mondragon, J.C.Wang |
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A 26 kDa yeast DNA topoisomerase I fragment: crystallographic structure and mechanistic implications. |
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1OO8 |
A.Dementiev, M.Simonovic, K.Volz, P.G.W.Gettins |
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Canonical Inhibitor-Like Interactions Explain Reactivity of Alpha-1-Pi Pittsburgh and Antithrombin with Proteinases |
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n/a |
1OPH |
A.Dementiev, M.Simonovic, K.Volz, P.G.W.Gettins |
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Canonical Inhibitor-Like Interactions Explain Reactivity of Alpha-1-Pi Pittsburgh and Antithrombin with Proteinases |
n/a |
n/a |
1OS1 |
A.Sudom, R.Walters, L.Pastushok, D.Goldie, L.Prasad, L.T.Delbaere, H.Goldie |
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1OS8 |
M.J.Page, S.L.Wong, J.Hewitt, N.C.Strynadka, R.T.Macgillivray |
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Biochemistry |
Engineering the Primary Substrate Specificity of Streptomyces Griseus Trypsin. |
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1OSS |
M.J.Page, S.L.Wong, J.Hewitt, N.C.Strynadka, R.T.Macgillivray |
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Biochemistry |
Engineering the Primary Substrate Specificity of Streptomyces Griseus Trypsin. |
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1OVA |
P.E.Stein, A.G.Leslie, J.T.Finch, R.W.Carrell |
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E.Papamokos, E.Weber, W.Bode, R.Huber, M.W.Empie, I.Kato, M.Laskowski Jr. |
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Crystallographic refinement of Japanese quail ovomucoid, a Kazal-type inhibitor, and model building studies of complexes with serine proteases. |
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H.Nar, M.Bauer, A.Schmid, J.Stassen, W.Wienen, H.W.Priepke, I.K.Kauffmann, U.J.Ries, N.H.Hauel |
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Structure |
Structural Basis for Inhibition Promiscuity of Dual Specific Thrombin and Factor Xa Blood Coagulation Inhibitors |
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2001 |
1P01 |
R.Bone, A.B.Shenvi, C.A.Kettner, D.A.Agard |
7609 |
3122831 |
Biochemistry |
Serine protease mechanism: structure of an inhibitory complex of alpha-lytic protease and a tightly bound peptide boronic acid. |
26 |
1987 |
1P02 |
R.Bone, D.Frank, C.A.Kettner, D.A.Agard |
7600 |
2611204 |
Biochemistry |
Structural analysis of specificity: alpha-lytic protease complexes with analogues of reaction intermediates. |
28 |
1989 |
1P03 |
R.Bone, D.Frank, C.A.Kettner, D.A.Agard |
7600 |
2611204 |
Biochemistry |
Structural analysis of specificity: alpha-lytic protease complexes with analogues of reaction intermediates. |
28 |
1989 |
1P04 |
R.Bone, D.Frank, C.A.Kettner, D.A.Agard |
7600 |
2611204 |
Biochemistry |
Structural analysis of specificity: alpha-lytic protease complexes with analogues of reaction intermediates. |
28 |
1989 |
1P05 |
R.Bone, D.Frank, C.A.Kettner, D.A.Agard |
7600 |
2611204 |
Biochemistry |
Structural analysis of specificity: alpha-lytic protease complexes with analogues of reaction intermediates. |
28 |
1989 |
1P06 |
R.Bone, D.Frank, C.A.Kettner, D.A.Agard |
7600 |
2611204 |
Biochemistry |
Structural analysis of specificity: alpha-lytic protease complexes with analogues of reaction intermediates. |
28 |
1989 |
1P09 |
R.Bone, J.L.Silen, D.A.Agard |
191 |
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Nature |
Structural plasticity broadens the specificity of an engineered protease. |
339 |
1989 |
1P10 |
R.Bone, J.L.Silen, D.A.Agard |
191 |
2716847 |
Nature |
Structural plasticity broadens the specificity of an engineered protease. |
339 |
1989 |
1P11 |
R.Bone, N.S.Sampson, P.A.Bartlett, D.A.Agard |
2263 |
1998685 |
Biochemistry |
Crystal structures of alpha-lytic protease complexes with irreversibly bound phosphonate esters. |
30 |
1991 |
1P12 |
R.Bone, N.S.Sampson, P.A.Bartlett, D.A.Agard |
2263 |
1998685 |
Biochemistry |
Crystal structures of alpha-lytic protease complexes with irreversibly bound phosphonate esters. |
30 |
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1PBI |
I.Li de la Sierra, L.Quillien, P.Flecker, J.Gueguen, S.Brunie |
1195 |
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Dimeric crystal structure of a Bowman-Birk protease inhibitor from pea seeds. |
285 |
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1PI2 |
P.Chen, J.Rose, R.Love, C.H.Wei, B.C.Wang |
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1730730 |
J Biol Chem |
Reactive sites of an anticarcinogenic Bowman-Birk proteinase inhibitor are similar to other trypsin inhibitors. |
267 |
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1PIT |
K.D.Berndt, P.Guntert, L.P.Orbons, K.Wuthrich |
757 |
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J Mol Biol |
Determination of a high-quality nuclear magnetic resonance solution structure of the bovine pancreatic trypsin inhibitor and comparison with three crystal structures. |
227 |
1992 |
1PMC |
G.Mer, H.Hietter, C.Kellenberger, M.Renatus, B.Luu, J.F.Lefevre |
158 |
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258 |
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1PPB |
W.Bode, I.Mayr, U.Baumann, R.Huber, S.R.Stone, J.Hofsteenge |
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The refined 1.9 A crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment. |
8 |
1989 |
1PPC |
W.Bode, D.Turk, J.Sturzebecher |
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Geometry of binding of the benzamidine- and arginine-based inhibitors N alpha-(2-naphthyl-sulphonyl-glycyl)-DL-p-amidinophenylalanyl-pipe ridine (NAPAP) and (2R,4R)-4-methyl-1-[N alpha-(3-methyl-1,2,3,4-tetrahydro-8- quinolinesulphonyl)-L-arginyl]-2-piperidine carboxylic acid (MQPA) to human alpha-thrombin. X-ray crystallographic determination of the NAPAP-trypsin complex and modeling of NAPAP-thrombin and MQPA-thrombin. |
193 |
1990 |
1PPE |
W.Bode, H.J.Greyling, R.Huber, J.Otlewski, T.Wilusz |
285 |
2914611 |
FEBS Lett |
The refined 2.0 A X-ray crystal structure of the complex formed between bovine beta-trypsin and CMTI-I, a trypsin inhibitor from squash seeds (Cucurbita maxima). Topological similarity of the squash seed inhibitors with the carboxypeptidase A inhibitor from potatoes. |
242 |
1989 |
1PPF |
W.Bode, A.Z.Wei, R.Huber, E.Meyer, J.Travis, S.Neumann |
2453 |
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X-ray crystal structure of the complex of human leukocyte elastase (PMN elastase) and the third domain of the turkey ovomucoid inhibitor. |
5 |
1986 |
1PPH |
D.Turk, J.Sturzebecher, W.Bode |
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1879520 |
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Geometry of binding of the N alpha-tosylated piperidides of m-amidino-, p-amidino- and p-guanidino phenylalanine to thrombin and trypsin. X-ray crystal structures of their trypsin complexes and modeling of their thrombin complexes. |
287 |
1991 |
1PSI |
P.R.Elliott, D.A.Lomas, R.W.Carrell, J.P.Abrahams |
676 |
8756325 |
Nat Struct Biol |
Inhibitory conformation of the reactive loop of alpha 1-antitrypsin. |
3 |
1996 |
1PXX |
S.W.Rowlinson, J.R.Kiefer, J.Prusakiewicz, J.L.Pawlitz, K.R.Kozak, A.S.Kalgutkar, W.C.Stallings, R.G.Kurumbail, L.J.Marnett |
n/a |
( 1PXX ) |
To be Published |
A Novel Mechanism of Cyclooxygenase-2 Inhibition Involving Interactions with Ser-530 and Tyr-385 |
n/a |
n/a |
1PYT |
F.X.Gomis-Ruth, M.Gomez, W.Bode, R.Huber, F.X.Aviles |
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7556081 |
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The three-dimensional structure of the native ternary complex of bovine pancreatic procarboxypeptidase A with proproteinase E and chymotrypsinogen C. |
14 |
1995 |
1Q0O |
M.W.Vetting, L.P.Wackett, L.Que, J.D.Lipscomb, D.H.Ohlendorf |
n/a |
( 1Q0O ) |
To be Published |
A Crystallographic Comparison of Manganese and Iron Dependent Homoprotocatechuate 2,3-Dioxygenase |
n/a |
n/a |
1QA0 |
M.Whitlow, D.O.Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QA0 ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QA7 |
E.M.Bergmann, M.M.Cherney, J.Mckendrick, J.C.Vederas, M.N.G.James |
153 |
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Virology |
Crystal Structure of an Inhibitor Complex of the 3C Proteinase from Hepatitis a Virus (Hav)and Implications for the Polyprotein Processing in Hav |
265 |
1999 |
1QB1 |
M.Whitlow, D.O Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QB1 ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QB6 |
M.Whitlow, D.O.Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QB6 ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QB9 |
M.Whitlow, D.O.Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QB9 ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QBN |
M.Whitlow, D.O Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QBN ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QBO |
M.Whitlow, D.O.Arnaiz, B.O.Buckman, D.D.Davey, B.Griedel, W.J.Guilford, S.K.Koovakkat, A.Liang, R.Mohan, G.B.Phillips, M.Seto, K.J.Shaw, W.Xu, Z.Zhao, D.R.Light, M.M.Morrissey |
1395 |
( 1QBO ) |
Acta Crystallogr., Sect.D |
Crystallographic Analysis of Potent and Selective Factor Xa Inhibitors Complexed to Bovine Trypsin |
55 |
1999 |
1QCP |
R.Recacha, M.Carson, M.J.Costanzo, B.Maryanoff, L.J.Delucas, D.Chattopadhyay |
1785 |
( 1QCP ) |
Acta Crystallogr., Sect.D |
Structure of the Rwj-51084-Bovine Pancreatic Beta-Trypsin Complex at 1.8 A |
55 |
1999 |
1QG1 |
K.Ogura, S.Tsuchiya, H.Terasawa, S.Yuzawa, H.Hatanaka, V.Mandiyan, J.Schlessinger, F.Inagaki |
439 |
( 1QG1 ) |
J.Mol.Biol. |
Solution Structure of the Sh2 Domain of Grb2 Complexed with the Shc Derived Phosphotyrosine Containing Peptide |
289 |
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1QH2 |
M.C.Lee, M.J.Scanlon, D.J.Craik, M.A.Anderson |
526 |
10360353 |
Nat Struct Biol |
A novel two-chain proteinase inhibitor generated by circularization of a multidomain precursor protein. |
6 |
1999 |
1QHR |
H.Jhoti, A.Cleasby, S.Reid, P.Thomas, M.Weir, A.Wonacott |
7969 |
( 1QHR ) |
Biochemistry |
Crystal Structures of Thrombin Complexed to a Novel Series of Synthetic Inhibitors Containing a 5,5-Trans-Lactone Template |
38 |
1999 |
1QIX |
R.C.Wilmouth, I.J.Clifton, C.V.Robinson, P.L.Roach, R.T.Aplin, N.J.Westwood, J.Hajdu, C.J.Schofield |
456 |
( 1QIX ) |
Nat.Struct.Biol. |
Structure of a Specific Acyl-Enzyme Complex Formed between Beta-Casomorphin-7 and Porcine Pancreatic Elastase |
4 |
1997 |
1QJ1 |
H.Jhoti, A.Cleasby, S.Reid, P.Thomas, M.Weir, A.Wonacott |
7969 |
( 1QJ1 ) |
Biochemistry |
Crystal Structures of Thrombin Complexed to a Novel Series of Synthetic Inhibitors Containing a 5,5-Trans-Lactone Template |
38 |
1999 |
1QJ6 |
H.Jhoti, A.Cleasby, S.Reid, P.Thomas, M.Weir, A.Wonacott |
7969 |
( 1QJ6 ) |
Biochemistry |
Crystal Structures of Thrombin Complexed to a Novel Series of Synthetic Inhibitors Containing a 5,5-Trans-Lactone Template |
38 |
1999 |
1QJ7 |
H.Jhoti, A.Cleasby, S.Reid, P.Thomas, M.Weir, A.Wonacott |
7969 |
( 1QJ7 ) |
Biochemistry |
Crystal Structures of Thrombin Complexed to a Novel Series of Synthetic Inhibitors Containing a 5,5-Trans-Lactone Template |
38 |
1999 |
1QL7 |
M.T.Stubbs, S.Reyda, F.Dullweber, M.Moeller, G.Klebe, K.D.Ullmann, H.D.Jakubke, D.Dorsch, W.W.K.R.Mederski, H.Wurzig |
n/a |
( 1QL7 ) |
To be Published |
A Case of Molecular Memory: Unexpected Binding Mode Induces a Factor Xa-Like Conformation in Trypsin |
n/a |
n/a |
1QL8 |
M.T.Stubbs, S.Reyda, F.Dullweber, M.Moeller, G.Klebe, K.D.Ullmann, H.D.Jakubke, D.Dorsch, W.W.K.R.Mederski, H.Wurzig |
n/a |
( 1QL8 ) |
To be Published |
A Case of Molecular Memory: Unexpected Binding Mode Induces a Factor Xa-Like Conformation in Trypsin |
n/a |
n/a |
1QL9 |
M.T.Stubbs, S.Reyda, F.Dullweber, M.Moeller, G.Klebe, K.D.Ullmann, H.D.Jakubke, D.Dorsch, W.W.K.R.Mederski, H.Wurziger |
n/a |
( 1QL9 ) |
To be Published |
A Case of Molecular Memory: Unexpected Binding Mode Induces a Factor Xa-Like Conformation in Trypsin |
n/a |
n/a |
1QLP |
P.R.Elliott, X.Y.Pei, T.Dafforn, D.A.Lomas |
1274 |
( 1QLP ) |
Protein Sci. |
Topography of a 2.0 A Structure of Alpha1-Antitrypsin Reveals Targets for Rational Drug Design to Prevent Conformational Disease. |
9 |
2000 |
1QLQ |
H.Czapinska, J.Otlewski, S.Krzywda, G.M.Sheldrick, M.Jaskolski |
1237 |
( 1QLQ ) |
J.Mol.Biol. |
High Resolution Structure of Bovine Pancreatic Trypsin Inhibitor with Altered Binding Loop Sequence |
295 |
1999 |
1QMB |
J.A.Huntington, N.S.Pannu, B.Hazes, R.J.Read, D.A.Lomas, R.W.Carrell |
449 |
( 1QMB ) |
J.Mol.Biol. |
A 2.6A Structure of a Serpin Polymer and Implications for Conformational Disease |
293 |
1999 |
1QMN |
B.Gooptu, B.Hazes, W.-S.W.Chang, T.R.Dafforn, R.W.Carrell, R.J.Read, D.A.Lomas |
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Proc.Nat.Acad.Sci.USA |
Inactive Conformation of the Serpin Alpha1-Antichymotrypsin Indicates Two- Stage Insertion of the Reactive Loop: Implications for Inhibitory Function and Conformational Disease |
97 |
2000 |
1QNJ |
M.Wurtele, M.Hahn, K.Hilpert, W.Hohne |
520 |
( 1QNJ ) |
Acta Crystallogr.,Sect.D |
Atomic Resolution Structure of Native Porcine Pancreatic Elastase at 1.1 A |
56 |
2000 |
1QQU |
A.Johnson, N.Gautham, V.Pattabhi |
7 |
( 1QQU ) |
Biochim.Biophys.Acta |
Crystal Structure at 1.63 A Resolution of the Native Form of Porcine Beta- Trypsin: Revealing an Acetate Ion Binding Site and Functional Water Network |
1435 |
1999 |
1QRZ |
E.Peisach, J.Wang, T.De Los Santos, E.Reich, D.Ringe |
11180 |
( 1QRZ ) |
Biochemistry |
Crystal Structure of the Proenzyme Domain of Plasminogen |
38 |
1999 |
1QUR |
T.Steinmetzer, M.Renatus, S.Kuenzel, A.Eichinger, W.Bode, P.Wikstroem, J.Hauptmann, J.Stuerzebecher |
598 |
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Eur.J.Biochem. |
Design and Evaluation of Novel Bivalent Thrombin Inhibitors Based on Amidinophenylalanines |
265 |
1999 |
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N.H.Keep, M.Barnes, I.Barsukov, R.Badii, L.Y.Lian, A.W.Segal, P.C.Moody, G.C.Roberts |
623 |
9195882 |
Structure |
A modulator of rho family G proteins, rhoGDI, binds these G proteins via an immunoglobulin-like domain and a flexible N-terminal arm. |
5 |
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1RTF |
D.Lamba, M.Bauer, R.Huber, S.Fischer, R.Rudolph, U.Kohnert, W.Bode |
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8613982 |
J Mol Biol |
The 2.3 A crystal structure of the catalytic domain of recombinant two-chain human tissue-type plasminogen activator. |
258 |
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1RTG |
U.Gohlke, F.X.Gomis-Ruth, T.Crabbe, G.Murphy, A.J.Docherty, W.Bode |
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FEBS Lett |
The C-terminal (haemopexin-like) domain structure of human gelatinase A (MMP2): structural implications for its function. |
378 |
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R.A.Alden, J.J.Birktoft, J.Kraut, J.D.Robertus, C.S.Wright |
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Biochem Biophys Res Commun |
Atomic coordinates for subtilisin BPN' (or Novo). |
45 |
1971 |
1SBW |
Y.Zhu, Q.Huang, C.Chi |
1219 |
10447205 |
J Biomol Struct Dyn |
Crystal structure of mung bean inhibitor lysine active fragment complex with bovine beta-trypsin at 1.8A resolution. |
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1SFI |
S.Luckett, R.S.Garcia, J.J.Barker, A.V.Konarev, P.Shewry, A.R.Clarke, R.L.Brady |
525 |
( 1SFI ) |
J.Mol.Biol. |
High Resolution Structure of a Potent, Cyclic Protease Inhibitor from Sunflower Seeds |
290 |
1999 |
1SGC |
L.T.Delbaere, G.D.Brayer |
89 |
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J.J.Birktoft, D.M.Blow |
187 |
( 2CHA ) |
J.Mol.Biol. |
The Structure of Crystalline Alpha-Chymotrypsin, V.The Atomic Structure of Tosyl-Alpha-Chymotrypsin at 2 Angstroms Resolution |
68 |
1972 |
2CI2 |
C.A.McPhalen, M.N.James |
261 |
3828302 |
Biochemistry |
Crystal and molecular structure of the serine proteinase inhibitor CI-2 from barley seeds. |
26 |
1987 |
2CTI |
T.A.Holak, D.Gondol, J.Otlewski, T.Wilusz |
635 |
2614837 |
J Mol Biol |
Determination of the complete three-dimensional structure of the trypsin inhibitor from squash seeds in aqueous solution by nuclear magnetic resonance and a combination of distance geometry and dynamical simulated annealing. |
210 |
1989 |
2EST |
D.L.Hughes, L.C.Sieker, J.Bieth, J.L.Dimicoli |
645 |
6926029 |
J Mol Biol |
Crystallographic study of the binding of a trifluoroacetyl dipeptide anilide inhibitor with elastase. |
162 |
1982 |
2ETI |
L.Chiche, C.Gaboriaud, A.Heitz, J.P.Mornon, B.Castro, P.A.Kollman |
405 |
2622910 |
Proteins |
Use of restrained molecular dynamics in water to determine three-dimensional protein structure: prediction of the three-dimensional structure of Ecballium elaterium trypsin inhibitor II. |
6 |
1989 |
2GCH |
G.H.Cohen, E.W.Silverton, D.R.Davies |
449 |
6914398 |
J Mol Biol |
Refined crystal structure of gamma-chymotrypsin at 1.9 A resolution. Comparison with other pancreatic serine proteases. |
148 |
1981 |
2GCT |
M.M.Dixon, R.G.Brennan, B.W.Matthews |
89 |
1888717 |
Int J Biol Macromol |
Structure of gamma-chymotrypsin in the range pH 2.0 to pH 10.5 suggests that gamma-chymotrypsin is a covalent acyl-enzyme adduct at low pH. |
13 |
1991 |
2GMT |
K.Kreutter, A.C.Steinmetz, T.C.Liang, M.Prorok, R.H.Abeles, D.Ringe |
13792 |
7947790 |
Biochemistry |
Three-dimensional structure of chymotrypsin inactivated with (2S)-N-acetyl-L-alanyl-L-phenylalanyl alpha-chloroethane: implications for the mechanism of inactivation of serine proteases by chloroketones. |
33 |
1994 |
2HEX |
J.Lubkowski, A.Wlodawer |
335 |
10089443 |
Acta Crystallogr D Biol Crystallogr |
Decamers observed in the crystals of bovine pancreatic trypsin inhibitor. |
55 |
1999 |
2HGT |
E.Skrzypczak-Jankun, V.E.Carperos, K.G.Ravichandran, A.Tulinsky, M.Westbrook, J.M.Maraganore |
1379 |
1942057 |
J Mol Biol |
Structure of the hirugen and hirulog 1 complexes of alpha-thrombin. |
221 |
1991 |
2HNT |
T.J.Rydel, M.Yin, K.P.Padmanabhan, D.T.Blankenship, A.D.Cardin, P.E.Correa, .2.Fenton 2nd, A.Tulinsky |
22000 |
8071320 |
J Biol Chem |
Crystallographic structure of human gamma-thrombin. |
269 |
1994 |
2HPP |
R.K.Arni, K.Padmanabhan, K.P.Padmanabhan, T.P.Wu, A.Tulinsky |
4727 |
8387813 |
Biochemistry |
Structures of the noncovalent complexes of human and bovine prothrombin fragment 2 with human PPACK-thrombin. |
32 |
1993 |
2HPQ |
R.K.Arni, K.Padmanabhan, K.P.Padmanabhan, T.P.Wu, A.Tulinsky |
4727 |
8387813 |
Biochemistry |
Structures of the noncovalent complexes of human and bovine prothrombin fragment 2 with human PPACK-thrombin. |
32 |
1993 |
2KAI |
Z.Chen, W.Bode |
283 |
( 2KAI ) |
J.Mol.Biol. |
Refined 2.5 Angstroms X-Ray Crystal Structure of the Complex Formed by Porcine Kallikrein a and the Bovine Pancreatic Trypsin Inhibitor. Crystallization, Patterson Search, Structure Determination, Refinement, Structure and Comparison with its Components and with the Bovine Trypsin-Pancreatic Trypsin Inhibitor Complex |
164 |
1983 |
2LET |
K.J.Nielsen, D.Alewood, J.Andrews, S.B.Kent, D.J.Craik |
291 |
8003965 |
Protein Sci |
An 1H NMR determination of the three-dimensional structures of mirror-image forms of a Leu-5 variant of the trypsin inhibitor from Ecballium elaterium (EETI-II). |
3 |
1994 |
2LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
2PKA |
W.Bode, Z.Chen, K.Bartels, C.Kutzbach, G.Schmidt-Kastner, H.Bartunik |
237 |
( 2PKA ) |
J.Mol.Biol. |
Refined 2 Angstroms X-Ray Crystal Structure of Porcine Pancreatic Kallikrein A, a Specific Trypsin-Like Serine Proteinase. Crystallization, Structure Determination, Crystallographic Refinement, Structure and its Comparison with Bovine Trypsin |
164 |
1983 |
2PTC |
M.Marquart, J.Walter, J.Deisenhofer, W.Bode, R.Huber |
480 |
( 2PTC ) |
Acta Crystallogr.,Sect.B |
The Geometry of the Reactive Site and of the Peptide Groups in Trypsin, Trypsinogen and its Complexes with Inhibitors |
39 |
1983 |
2PTN |
J.Walter, W.Steigemann, T.P.Singh, H.Bartunik, W.Bode, R.Huber |
1462 |
( 2PTN ) |
Acta Crystallogr.,Sect.B |
On the Disordered Activation Domain in Trypsinogen. Chemical Labelling and Low-Temperature Crystallography |
38 |
1982 |
2SEC |
C.A.McPhalen, M.N.James |
6582 |
3064813 |
Biochemistry |
Structural comparison of two serine proteinase-protein inhibitor complexes: eglin-c-subtilisin Carlsberg and CI-2-subtilisin Novo. |
27 |
1988 |
2SGA |
J.Moult, F.Sussman, M.N.James |
555 |
3892015 |
J Mol Biol |
Electron density calculations as an extension of protein structure refinement. Streptomyces griseus protease A at 1.5 A resolution. |
182 |
1985 |
2SNI |
C.A.McPhalen, M.N.James |
6582 |
3064813 |
Biochemistry |
Structural comparison of two serine proteinase-protein inhibitor complexes: eglin-c-subtilisin Carlsberg and CI-2-subtilisin Novo. |
27 |
1988 |
2SNV |
L.Tong, G.Wengler, M.G.Rossmann |
228 |
( 2SNV ) |
J.Mol.Biol. |
The Refined Structure of Sindbis Virus Core Protein in Comparison with Other Chymotrypsin-Like Serine Proteinase Structures |
230 |
1993 |
2SNW |
H.K.Choi, S.Lee, Y.P.Zhang, B.R.McKinney, G.Wengler, M.G.Rossmann, R.J.Kuhn |
151 |
8831786 |
J Mol Biol |
Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis. |
262 |
1996 |
2STA |
R.Helland, G.I.Berglund, J.Otlewski, W.Apostoluk, O.A.Andersen, N.P.Willassen, A.O.Smalas |
139 |
( 2STA ) |
Acta Crystallogr., Sect.D |
High-Resolution Structures of Three New Trypsin-Squash-Inhibitor Complexes: A Detailed Comparison with Other Trypsins and Their Complexes |
55 |
1999 |
2STB |
R.Helland, G.I.Berglund, J.Otlewski, W.Apostoluk, O.A.Andersen, N.P.Willassen, A.O.Smalas |
139 |
( 2STB ) |
Acta Crystallogr., Sect.D |
High-Resolution Structures of Three New Trypsin-Squash-Inhibitor Complexes: A Detailed Comparison with Other Trypsins and Their Complexes |
55 |
1999 |
2TBS |
A.O.Smalas, E.S.Heimstad, A.Hordvik, N.P.Willassen, R.Male |
149 |
7846025 |
Proteins |
Cold adaption of enzymes: structural comparison between salmon and bovine trypsins. |
20 |
1994 |
2TGA |
J.Walter, W.Steigemann, T.P.Singh, H.Bartunik, W.Bode, R.Huber |
1462 |
( 2TGA ) |
Acta Crystallogr.,Sect.B |
On the Disordered Activation Domain in Trypsinogen. Chemical Labelling and Low-Temperature Crystallography |
38 |
1982 |
2TGD |
M.O.Jones, R.M.Stroud |
n/a |
( 2TGD ) |
To be Published |
Lack of the Transition State Stabilization Site is a Factor in the Inactivity of Trypsinogen, a Serine Protease Zymogen. Structure of /Dfp Inhibited Bovine Trypsinogen at 2.1 Angstroms Resolution |
n/a |
n/a |
2TGP |
M.Marquart, J.Walter, J.Deisenhofer, W.Bode, R.Huber |
480 |
( 2TGP ) |
Acta Crystallogr.,Sect.B |
The Geometry of the Reactive Site and of the Peptide Groups in Trypsin, Trypsinogen and its Complexes with Inhibitors |
39 |
1983 |
2TGT |
J.Walter, W.Steigemann, T.P.Singh, H.Bartunik, W.Bode, R.Huber |
1462 |
( 2TGT ) |
Acta Crystallogr.,Sect.B |
On the Disordered Activation Domain in Trypsinogen. Chemical Labelling and Low-Temperature Crystallography |
38 |
1982 |
2THF |
E.R.Guinto, S.Caccia, T.Rose, K.Futterer, G.Waksman, E.Di Cera |
1852 |
10051558 |
Proc Natl Acad Sci U S A |
Unexpected crucial role of residue 225 in serine proteases. |
96 |
1999 |
2TIO |
G.Zhu, Q.Huang, Z.Wang, M.Qian, Y.Jia, Y.Tang |
142 |
9920392 |
Biochim Biophys Acta |
X-ray studies on two forms of bovine beta-trypsin crystals in neat cyclohexane. |
1429 |
1998 |
2TLD |
Y.Takeuchi, T.Nonaka, K.T.Nakamura, S.Kojima, K.Miura, Y.Mitsui |
4407 |
1584773 |
Proc Natl Acad Sci U S A |
Crystal structure of an engineered subtilisin inhibitor complexed with bovine trypsin. |
89 |
1992 |
2TPI |
J.Walter, W.Steigemann, T.P.Singh, H.Bartunik, W.Bode, R.Huber |
1462 |
( 2TPI ) |
Acta Crystallogr.,Sect.B |
On the Disordered Activation Domain in Trypsinogen. Chemical Labelling and Low-Temperature Crystallography |
38 |
1982 |
2TRM |
S.Sprang, T.Standing, R.J.Fletterick, R.M.Stroud, J.Finer-Moore, N.H.Xuong, R.Hamlin, W.J.Rutter, C.S.Craik |
905 |
3112942 |
Science |
The three-dimensional structure of Asn102 mutant of trypsin: role of Asp102 in serine protease catalysis. |
237 |
1987 |
2VGC |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
2WBC |
J.K.Dattagupta, A.Podder, C.Chakrabarti, U.Sen, S.K.Dutta, M.Singh |
521 |
( 2WBC ) |
Acta Crystallogr.,Sect.D |
Structure of a Kunitz-Type Chymotrypsin from Winged Bean Seeds at 2.95 A Resolution |
52 |
1996 |
3BTD |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTD ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTE |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTE ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTF |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTF ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTG |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTG ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTH |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTH ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTK |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTK ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTM |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTM ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTQ |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTQ ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTT |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTT ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3BTW |
R.Helland, J.Otlewski, O.Sundheim, M.Dadlez, A.O.Smalas |
923 |
( 3BTW ) |
J.Mol.Biol. |
The Crystal Structures of the Complexes between Bovine Beta-Trypsin and Ten P1 Variants of Bpti |
287 |
1999 |
3CAA |
C.M.Lukacs, J.Q.Zhong, M.I.Plotnick, H.Rubin, B.S.Cooperman, D.W.Christianson |
888 |
8836107 |
Nat Struct Biol |
Arginine substitutions in the hinge region of antichymotrypsin affect serpin beta-sheet rearrangement. |
3 |
1996 |
3CI2 |
S.Ludvigsen, H.Y.Shen, M.Kjaer, J.C.Madsen, F.M.Poulsen |
621 |
1748996 |
J Mol Biol |
Refinement of the three-dimensional solution structure of barley serine proteinase inhibitor 2 and comparison with the structures in crystals. |
222 |
1991 |
3CTI |
M.Nilges, J.Habazettl, A.T.Brunger, T.A.Holak |
499 |
2051485 |
J Mol Biol |
Relaxation matrix refinement of the solution structure of squash trypsin inhibitor. |
219 |
1991 |
3EST |
E.Meyer, G.Cole, R.Radhakrishnan, O.Epp |
26 |
3271103 |
Acta Crystallogr B |
Structure of native porcine pancreatic elastase at 1.65 A resolutions. |
44 |
1988 |
3GCH |
B.L.Stoddard, J.Bruhnke, N.Porter, D.Ringe, G.A.Petsko |
n/a |
( 3GCH ) |
To be Published |
Chemistry of Caged Enzymes. Binding of Photoreversible Cinnamates to Chymotrypsin |
n/a |
n/a |
3GCT |
M.M.Dixon, R.G.Brennan, B.W.Matthews |
89 |
1888717 |
Int J Biol Macromol |
Structure of gamma-chymotrypsin in the range pH 2.0 to pH 10.5 suggests that gamma-chymotrypsin is a covalent acyl-enzyme adduct at low pH. |
13 |
1991 |
3HAT |
I.I.Mathews, A.Tulinsky |
n/a |
( 3HAT ) |
To be Published |
Active Site Mimetic Inhibition of Thrombin |
n/a |
n/a |
3HTC |
T.Rydel, K.G.Ravichandran, A.Tulinsky, W.Bode, R.Huber, C.Roitsch, J.W.Fenton /II |
277 |
( 3HTC ) |
Science |
The Structure of a Complex of Recombinant Hirudin and Human Alpha-Thrombin |
249 |
1990 |
3LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
3PTB |
M.Marquart, J.Walter, J.Deisenhofer, W.Bode, R.Huber |
480 |
( 3PTB ) |
Acta Crystallogr.,Sect.B |
The Geometry of the Reactive Site and of the Peptide Groups in Trypsin, Trypsinogen and its Complexes with Inhibitors |
39 |
1983 |
3PTN |
J.Walter, W.Steigemann, T.P.Singh, H.Bartunik, W.Bode, R.Huber |
1462 |
( 3PTN ) |
Acta Crystallogr.,Sect.B |
On the Disordered Activation Domain in Trypsinogen. Chemical Labelling and Low-Temperature Crystallography |
38 |
1982 |
3RP2 |
S.J.Remington, R.G.Woodbury, R.A.Reynolds, B.W.Matthews, H.Neurath |
8097 |
3233198 |
Biochemistry |
The structure of rat mast cell protease II at 1.9-A resolution. |
27 |
1988 |
3SGA |
M.N.James, A.R.Sielecki, G.D.Brayer, L.T.Delbaere, C.A.Bauer |
43 |
6783761 |
J Mol Biol |
Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis. |
144 |
1980 |
3SGB |
R.J.Read, M.Fujinaga, A.R.Sielecki, M.N.G.James |
4420 |
( 3SGB ) |
Biochemistry |
Structure of the Complex of Streptomyces Griseus Protease B and the Third Domain of the Turkey Ovomucoid Inhibitor at 1.8 Angstroms Resolution |
22 |
1983 |
3SSI |
T.Suzuki |
n/a |
( 3SSI ) |
To be Published |
Structural Modulation of the Protein Proteinase Inhibitor Ssi (Streptomyces Subtilisin Inhibitor) |
n/a |
n/a |
3TGI |
A.Pasternak, D.Ringe, L.Hedstrom |
n/a |
( 3TGI ) |
To be Published |
Comparison of Anionic and Cationic Trypsinogens: The Anionic Activation Domain is More Flexible in Solution and Differs in its Mode of Bpti Binding in the Crystal Structure |
n/a |
n/a |
3TGJ |
A.Pasternak, D.Ringe, L.Hedstrom |
n/a |
( 3TGJ ) |
To be Published |
Comparison of Anionic and Cationic Trypsinogens: The Anionic Activation Domain is More Flexible in Solution and Differs in its Mode of Bpti Binding in the Crystal Structure |
n/a |
n/a |
3TGK |
A.Pasternak, A.White, C.J.Jeffery, N.Medina, M.Cahoon, D.Ringe, L.Hedstrom |
1331 |
( 3TGK ) |
Protein Sci. |
The Energetic Cost of Induced Fit Catalysis: Crystal Structures of Trypsinogen Mutants with Enhanced Activity and Inhibitor Affinity |
10 |
2001 |
3TPI |
M.Marquart, J.Walter, J.Deisenhofer, W.Bode, R.Huber |
480 |
( 3TPI ) |
Acta Crystallogr.,Sect.B |
The Geometry of the Reactive Site and of the Peptide Groups in Trypsin, Trypsinogen and its Complexes with Inhibitors |
39 |
1983 |
3VGC |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
3VSB |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
4CAA |
C.M.Lukacs, J.Q.Zhong, M.I.Plotnick, H.Rubin, B.S.Cooperman, D.W.Christianson |
888 |
8836107 |
Nat Struct Biol |
Arginine substitutions in the hinge region of antichymotrypsin affect serpin beta-sheet rearrangement. |
3 |
1996 |
4CHA |
H.Tsukada, D.M.Blow |
703 |
4046030 |
J Mol Biol |
Structure of alpha-chymotrypsin refined at 1.68 A resolution. |
184 |
1985 |
4EST |
L.H.Takahashi, R.Radhakrishnan, R.E.Rosenfield Jr., E.F.Meyer Jr. |
7610 |
2611205 |
Biochemistry |
Crystallographic analysis of the inhibition of porcine pancreatic elastase by a peptidyl boronic acid: structure of a reaction intermediate. |
28 |
1989 |
4GCH |
B.L.Stoddard, J.Bruhnke, N.Porter, D.Ringe, G.A.Petsko |
4871 |
2364065 |
Biochemistry |
Structure and activity of two photoreversible cinnamates bound to chymotrypsin. |
29 |
1990 |
4HTC |
T.J.Rydel, A.Tulinsky, W.Bode, R.Huber |
583 |
( 4HTC ) |
J.Mol.Biol. |
The Refined Structure of the Hirudin-Thrombin Complex |
221 |
1991 |
4PTI |
M.Marquart, J.Walter, J.Deisenhofer, W.Bode, R.Huber |
480 |
( 4PTI ) |
Acta Crystallogr.,Sect.B |
The Geometry of the Reactive Site and of the Peptide Groups in Trypsin, Trypsinogen and its Complexes with Inhibitors |
39 |
1983 |
4SGA |
M.N.James, A.R.Sielecki, G.D.Brayer, L.T.Delbaere, C.A.Bauer |
43 |
6783761 |
J Mol Biol |
Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis. |
144 |
1980 |
4SGB |
H.M.Greenblatt, C.A.Ryan, M.N.James |
201 |
2494344 |
J Mol Biol |
Structure of the complex of Streptomyces griseus proteinase B and polypeptide chymotrypsin inhibitor-1 from Russet Burbank potato tubers at 2.1 A resolution. |
205 |
1989 |
4TPI |
W.Bode, J.Walter, R.Huber, H.R.Wenzel, H.Tschesche |
185 |
( 4TPI ) |
Eur.J.Biochem. |
The Refined 2.2-Angstroms (0.22-Nm) X-Ray Crystal Structure of the Ternary Complex Formed by Bovine Trypsinogen, Valine-Valine and the Arg==15== Analogue of Bovine Pancreatic Trypsin Inhibitor |
144 |
1984 |
4VGC |
V.S.Stoll, B.T.Eger, R.C.Hynes, V.Martichonok, J.B.Jones, E.F.Pai |
451 |
9425066 |
Biochemistry |
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes. |
37 |
1998 |
4WBC |
S.Ravichandran, U.Sen, C.Chakrabarti, J.K.Dattagupta |
1814 |
( 4WBC ) |
Acta Crystallogr., Sect.D |
Cryocrystallography of a Serine Protease Inhibitor: The 90 K Structure of Winged Bean Chymotrypsin Inhibitor (Wci) at 2.13 A Resolution |
55 |
1999 |
5CHA |
R.A.Blevins, A.Tulinsky |
4264 |
3980476 |
J Biol Chem |
The refinement and the structure of the dimer of alpha-chymotrypsin at 1.67-A resolution. |
260 |
1985 |
5EST |
L.H.Takahashi, R.Radhakrishnan, R.E.Rosenfield Jr., E.F.Meyer Jr. |
7610 |
2611205 |
Biochemistry |
Crystallographic analysis of the inhibition of porcine pancreatic elastase by a peptidyl boronic acid: structure of a reaction intermediate. |
28 |
1989 |
5GCH |
B.L.Stoddard, J.Bruhnke, P.Koenig, N.Porter, D.Ringe, G.A.Petsko |
n/a |
( 5GCH ) |
To be Published |
Chemistry of Caged Enzymes /II. Photoactivation of Inhibited Chymotrypsin |
n/a |
n/a |
5GDS |
G.De Simone, A.Lombardi, S.Galdiero, F.Nastri, R.Della Morte, N.Staiano, C.Pedone, M.Bolognesi, V.Pavone |
243 |
9521099 |
Protein Sci |
Hirunorms are true hirudin mimetics. The crystal structure of human alpha-thrombin-hirunorm V complex. |
7 |
1998 |
5LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
5PTI |
A.Wlodawer, J.Walter, R.Huber, L.Sjolin |
301 |
6210373 |
J Mol Biol |
Structure of bovine pancreatic trypsin inhibitor. Results of joint neutron and X-ray refinement of crystal form II. |
180 |
1984 |
5PTP |
J.S.Finer-Moore, A.A.Kossiakoff, J.H.Hurley, T.Earnest, R.M.Stroud |
203 |
1557349 |
Proteins |
Solvent structure in crystals of trypsin determined by X-ray and neutron diffraction. |
12 |
1992 |
5SGA |
M.N.James, A.R.Sielecki, G.D.Brayer, L.T.Delbaere, C.A.Bauer |
43 |
6783761 |
J Mol Biol |
Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis. |
144 |
1980 |
6CHA |
A.Tulinsky, R.A.Blevins |
7737 |
3584139 |
J Biol Chem |
Structure of a tetrahedral transition state complex of alpha-chymotrypsin dimer at 1.8-A resolution. |
262 |
1987 |
6EST |
I.Li De La Sierra, E.Papamichael, C.Sakarelos, J.-L.Dimicoli, T.Prange |
36 |
( 6EST ) |
J.Mol.Recog. |
Interaction of the Peptide /Cf3-Leu-Ala-/Nh-C6H4-Cf3(/Tfla) with Porcine Pancreatic Elastase. X-Ray Studies at 1.8 Angstroms |
3 |
1990 |
6GCH |
K.Brady, A.Z.Wei, D.Ringe, R.H.Abeles |
7600 |
2271520 |
Biochemistry |
Structure of chymotrypsin-trifluoromethyl ketone inhibitor complexes: comparison of slowly and rapidly equilibrating inhibitors. |
29 |
1990 |
6LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
6PTI |
A.Wlodawer, J.Nachman, G.L.Gilliland, W.Gallagher, C.Woodward |
469 |
2448484 |
J Mol Biol |
Structure of form III crystals of bovine pancreatic trypsin inhibitor. |
198 |
1987 |
7API |
R.Engh, H.Lobermann, M.Schneider, G.Wiegand, R.Huber, C.B.Laurell |
407 |
2785270 |
Protein Eng |
The S variant of human alpha 1-antitrypsin, structure and implications for function and metabolism. |
2 |
1989 |
7EST |
I.Li De La Sierra, E.Papamichael, C.Sakarelos, J.-L.Dimicoli, T.Prange |
36 |
( 7EST ) |
J.Mol.Recog. |
Interaction of the Peptide /Cf3-Leu-Ala-/Nh-C6H4-Cf3(/Tfla) with Porcine Pancreatic Elastase. X-Ray Studies at 1.8 Angstroms |
3 |
1990 |
7GCH |
K.Brady, A.Z.Wei, D.Ringe, R.H.Abeles |
7600 |
2271520 |
Biochemistry |
Structure of chymotrypsin-trifluoromethyl ketone inhibitor complexes: comparison of slowly and rapidly equilibrating inhibitors. |
29 |
1990 |
7LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
7PTI |
C.Eigenbrot, M.Randal, A.A.Kossiakoff |
591 |
1699222 |
Protein Eng |
Structural effects induced by removal of a disulfide-bridge: the X-ray structure of the C30A/C51A mutant of basic pancreatic trypsin inhibitor at 1.6 A. |
3 |
1990 |
8API |
R.Engh, H.Lobermann, M.Schneider, G.Wiegand, R.Huber, C.B.Laurell |
407 |
2785270 |
Protein Eng |
The S variant of human alpha 1-antitrypsin, structure and implications for function and metabolism. |
2 |
1989 |
8EST |
J.C.Powers, J.Oleksyszyn, S.L.Narasimhan, C.M.Kam |
3108 |
2337582 |
Biochemistry |
Reaction of porcine pancreatic elastase with 7-substituted 3-alkoxy-4-chloroisocoumarins: design of potent inhibitors using the crystal structure of the complex formed with 4-chloro-3-ethoxy-7-guanidinoisocoumarin. |
29 |
1990 |
8GCH |
M.Harel, C.T.Su, F.Frolow, I.Silman, J.L.Sussman |
5217 |
2036388 |
Biochemistry |
Gamma-chymotrypsin is a complex of alpha-chymotrypsin with its own autolysis products. |
30 |
1991 |
8LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
8PTI |
D.Housset, K.S.Kim, J.Fuchs, C.Woodward, A.Wlodawer |
757 |
1714504 |
J Mol Biol |
Crystal structure of a Y35G mutant of bovine pancreatic trypsin inhibitor. |
220 |
1991 |
9API |
R.Engh, H.Lobermann, M.Schneider, G.Wiegand, R.Huber, C.B.Laurell |
407 |
2785270 |
Protein Eng |
The S variant of human alpha 1-antitrypsin, structure and implications for function and metabolism. |
2 |
1989 |
9EST |
J.Vijayalakshmi, E.F.Meyer Jr., C.M.Kam, J.C.Powers |
2175 |
1998677 |
Biochemistry |
Structural study of porcine pancreatic elastase complexed with 7-amino-3-(2-bromoethoxy)-4-chloroisocoumarin as a nonreactivatable doubly covalent enzyme-inhibitor complex. |
30 |
1991 |
9LPR |
R.Bone, A.Fujishige, C.A.Kettner, D.A.Agard |
10388 |
1931963 |
Biochemistry |
Structural basis for broad specificity in alpha-lytic protease mutants. |
30 |
1991 |
9PTI |
C. Eigenbrot, M. Randal, A. A. Kossiakoff |
n/a |
( 9PTI ) |
n/a |
Crystal structure of a Y35G mutant of bovine pancreatic trypsin inhibitor |
n/a |
n/a |
|