|
64
|
234
|
4y6dA |
Factor xa complex with gtc000101 |
|
114
|
471
|
4xd7D |
Structure of thermophilic f1-atpase inhibited by epsilon subunit |
|
40
|
183
|
4xbcA |
1.60 a resolution structure of norovirus 3cl protease complex with a covalently bound dipeptidyl inhibitor (1r,2s)-2-({n-[(benzyloxy)carbonyl]-3-cyclohexyl-l-alanyl}amino)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propane-1-sulfonic acid (hexagonal form) |
|
57
|
223
|
4y10E |
Trypsin in complex with with bpti mutant (2s)-2-amino-4,4-difluorobutanoic acid |
|
39
|
175
|
4xbbA |
1.85a resolution structure of norovirus 3cl protease complex with a covalently bound dipeptidyl inhibitor diethyl [(1r,2s)-2-[(n-{[(3-chlorobenzyl)oxy]carbonyl}-3-cyclohexyl-l-alanyl)amino]-1-hydroxy-3-(2-oxo-2h-pyrrol-3-yl)propyl]phosphonate |
|
68
|
234
|
4y7aA |
Factor xa complex with gtc000422 |
|
18
|
104
|
4xrnA |
Pilz domain with c-di-gmp of a protein from pseudomonas aeruginosa |
|
85
|
298
|
4xfqA |
Crystal structure basis for pedv 3c like protease |
|
54
|
236
|
4x6pA |
Factor xia (pichia pastoris; c500s [c122s]) in complex with the inhibitor (2e)-n-{(1s)-1-[4-(3-amino-1h-indazol-6-yl)-1h-imidazol-2-yl]-2-phenylethyl}-3-[5-chloro-2-(1h-tetrazol-1-yl)phenyl]prop-2-enamide |
|
28
|
176
|
4x2xA |
Crystal structure of the murine norovirus ns6 protease (inactive c139a mutant) with a c-terminal extension to include residues p1 prime - p4 prime of ns7 |
|
59
|
246
|
4x1sU |
The crystal structure of mupain-1-16-d9a in complex with murinised human upa at ph7.4 |
|
58
|
314
|
4wjg2 |
Structure of t. brucei haptoglobin-hemoglobin receptor binding to human haptoglobin-hemoglobin |
|
20
|
95
|
4vgcC |
Gamma-chymotrypsin d-naphthyl-1-acetamido boronic acid inhibitor complex |
|
85
|
305
|
4wmfA |
Crystal structure of catalytically inactive mers-cov 3cl protease (c148a) in spacegroup p212121 |
|
49
|
238
|
4wxiA |
Factor xia in complex with the inhibitor trans-n-{(1s)-1-[4-(3-amino-2h-indazol-6-yl)pyridin-2-yl]-2-phenylethyl}-4-(aminomethyl)cyclohexanecarboxamide |
|
16
|
131
|
4vgcB |
Gamma-chymotrypsin d-naphthyl-1-acetamido boronic acid inhibitor complex |
|
58
|
247
|
4x1nU |
The crystal structure of mupain-1-16 in complex with murinised human upa at ph7.4 |
|
85
|
306
|
4wmeA |
Crystal structure of catalytically inactive mers-cov 3cl protease (c148a) in spacegroup c2 |
|
43
|
192
|
4wf8A |
Crystal structure of ns3/4a protease in complex with asunaprevir |
|
58
|
254
|
4x8vH |
Factor viia in complex with the inhibitor (methyl {3-[(2r)-1-{(2r)-2-(3,4-dimethoxyphenyl)-2-[(1-oxo-1,2,3,4-tetrahydroisoquinolin-7-yl)amino]acetyl}pyrrolidin-2-yl]-4-(propan-2-ylsulfonyl)phenyl}carbamate) |
|
45
|
218
|
4wvpE |
Crystal structure of an activity-based probe hne complex |
|
49
|
198
|
4wh8A |
Crystal structure of hcv ns3/4a protease in complex with an asunaprevir p1-p3 macrocyclic analog. |
|
60
|
224
|
4wxvA |
Human cationic trypsin k97d mutant in complex with bovine pancreatic trypsin inhibitor (bpti) |
|
52
|
238
|
4x6mA |
Factor xia in complex with the inhibitor 1-{(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl}-3-[2-(aminomethyl)-5-chlorobenzyl]urea |
|
55
|
247
|
4x0wU |
The crystal structure of mupain-1-17 in complex with murinised human upa |
|
81
|
306
|
4wy3A |
Structure of sars-3cl protease complex with a phenylbenzoyl (r,s)-n-decalin type inhibitor |
|
57
|
247
|
4x1qU |
The crystal structure of mupain-1 in complex with murinised human upa at ph7.4 |
|
51
|
200
|
4wh6A |
Crystal structure of hcv ns3/4a protease variant r155k in complex with asunaprevir |
|
59
|
254
|
4x8tH |
Factor viia in complex with the inhibitor 7-chloro-3,4-dihydroisoquinolin-1(2h)-one |
|
53
|
238
|
4x6oA |
Factor xia in complex with the inhibitor methyl (4-{4-chloro-2-[(1s)-1-({3-[5-chloro-2-(1h-tetrazol-1-yl)phenyl]propanoyl}amino)-2-phenylethyl]-1h-imidazol-5-yl}phenyl)carbamate |
|
29
|
179
|
4x2wA |
Crystal structure of the murine norovirus ns6 protease (inactive c139a mutant) with a c-terminal extension to include residues p1 prime - p2 prime of ns7 |
|
29
|
179
|
4x2yA |
Crystal structure of a chimeric murine norovirus ns6 protease (inactive c139a mutant) in which the p4-p4 prime residues of the cleavage junction in the extended c-terminus have been replaced by the corresponding residues from the ns2-3 junction. |
|
85
|
301
|
4wmdA |
Crystal structure of catalytically inactive mers-cov 3cl protease (c148a) in spacegroup c2221 |
|
59
|
254
|
4x8uH |
Factor viia in complex with the inhibitor 5-chloro-1h-indole-2-carboxylic acid |
|
56
|
247
|
4x1pU |
The crystal structure of mupain-1-17 in complex with murinised human upa at ph4.6 |
|
56
|
224
|
4wwyA |
Human cationic trypsin g193r mutant in complex with bovine pancreatic trypsin inhibitor |
|
55
|
238
|
4x6nA |
Factor xia in complex with the inhibitor 1-{(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl}-3-[5-chloro-2-(1h-tetrazol-1-yl)benzyl]urea |
|
30
|
174
|
4x2vA |
Crystal structure of the murine norovirus ns6 protease (inactive c139a mutant) with a c-terminal extension to include residue p1 prime of ns7 |
|
56
|
247
|
4x1rU |
The crystal structure of mupain-1-12 in complex with murinised human upa at ph7.4 |
|
58
|
258
|
4ufeH |
Thrombin in complex with (2r)-2-(benzylsulfonylamino)-n-(2-((4- carbamimidoylphenyl)methylamino)-2-oxo-butyl)-3-phenyl-propanamide |
|
56
|
258
|
4ue7H |
Thrombin in complex with 1-amidinopiperidine |
|
60
|
223
|
4u2wA |
Atomic resolution crystal structure of hv-bbi protease inhibitor from amphibian skin in complex with bovine trypsin |
|
53
|
238
|
4ty7A |
Factor xia in complex with the inhibitor (2s)-6-amino-n-{(1s)-1-[4-(3-amino-2h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl}-2-ethylhexanamide |
|
53
|
223
|
4tpiZ |
The refined 2.2-angstroms (0.22-nm) x-ray crystal structure of the ternary complex formed by bovine trypsinogen, valine-valine and the arg15 analogue of bovine pancreatic trypsin inhibitor |
|
46
|
198
|
4tydA |
Structure-based design of a novel series of azetidine inhibitors of the hepatitis c virus ns3/4a serine protease |
|
51
|
259
|
4thnH |
The crystal structure of alpha-thrombin-hirunorm iv complex reveals a novel specificity site recognition mode. |
|
56
|
224
|
4u32A |
Human mesotrypsin complexed with hai-2 kunitz domain 1 |
|
49
|
185
|
4sgbE |
Structure of the complex of streptomyces griseus proteinase b and polypeptide chymotrypsin inhibitor-1 from russet burbank potato tubers at 2.1 angstroms resolution |
|
58
|
258
|
4ufdH |
Thrombin in complex with 4-(((1-((2s)-1-((2r)-2-(benzylsulfonylamino)- 3-phenyl-propanoyl)pyrrolidin-2-yl)-1-oxo-ethyl)amino)methyl) benzamidine |
|
57
|
258
|
4ufgH |
Thrombin in complex with (2r)-2-(benzylsulfonylamino)-n-((1s)-2-((4- carbamimidoylphenyl)methylamino)-1-methyl-2-oxo-ethyl)-n-methyl-3- phenyl-propanamide ethane |
