|
19
|
96
|
3ru4E |
Crystal structure of the bowman-birk serine protease inhibitor btci in complex with trypsin and chymotrypsin |
|
55
|
223
|
3rxrA |
Crystal structure of trypsin complexed with cycloheptanamine (f01 and f03, cocktail experiment) |
|
57
|
223
|
3rxjA |
Crystal structure of trypsin complexed with 4-guanidinobenzoic acid |
|
56
|
223
|
3rxiA |
Crystal structure of trypsin complexed with 2-(1h-indol-3-yl)ethanamine |
|
42
|
184
|
3ruoA |
Complex structure of hevb ev93 main protease 3c with rupintrivir (ag7088) |
|
57
|
223
|
3rxgA |
Crystal structure of trypsin complexed with 4-aminocyclohexanol |
|
57
|
223
|
3rxbA |
Crystal structure of trypsin complexed with 4-guanidinobutanoic acid |
|
54
|
223
|
3rxuA |
Crystal structure of trypsin complexed with benzamide (f05 and a06, cocktail experiment) |
|
57
|
258
|
3rmmH |
Human thrombin in complex with mi332 |
|
59
|
258
|
3rm2H |
Human thrombin in complex with mi003 |
|
58
|
258
|
3rmoH |
Human thrombin in complex with mi004 |
|
58
|
258
|
3rlwH |
Human thrombin in complex with mi328 |
|
59
|
258
|
3rmnH |
Human thrombin in complex with mi341 |
|
59
|
258
|
3rlyH |
Human thrombin in complex with mi329 |
|
50
|
224
|
3rp2A |
The structure of rat mast cell protease ii at 1.9-angstroms resolution |
|
58
|
258
|
3rmlH |
Human thrombin in complex with mi331 |
|
60
|
258
|
3rm0H |
Human thrombin in complex with mi354 |
|
52
|
202
|
3rc6A |
Molecular mechanisms of viral and host-cell substrate recognition by hcv ns3/4a protease |
|
49
|
199
|
3rc4A |
Molecular mechanisms of viral and host-cell substrate recognition by hcv ns3/4a protease |
|
48
|
198
|
3rc5A |
Molecular mechanisms of viral and host-cell substrate recognition by hcv ns3/4a protease |
|
55
|
223
|
3rdzA |
Crystal structure of rbti-trypsin complex at 2.26 angstrom resolution |
|
203
|
734
|
2ok5A |
Human complement factor b |
|
82
|
305
|
2q6gA |
Crystal structure of sars-cov main protease h41a mutant in complex with an n-terminal substrate |
|
54
|
200
|
2w7sA |
Spla serine protease of staphylococcus aureus (1.8a) |
|
57
|
236
|
5tjxA |
Structure of human plasma kallikrein |
|
60
|
228
|
5tccA |
Complement factor d inhibited with jh4 |
|
33
|
174
|
5t6gA |
2.45 a resolution structure of norovirus 3cl protease in complex with the dipeptidyl inhibitor 7m (hexagonal form) |
|
63
|
228
|
5tcaA |
Complement factor d inhibited with jh3 |
|
40
|
175
|
5t6dA |
2.10 a resolution structure of norovirus 3cl protease in complex with the dipeptidyl inhibitor 7l (hexagonal form) |
|
38
|
174
|
5t6fA |
1.90 a resolution structure of norovirus 3cl protease in complex with the dipeptidyl inhibitor 7l (orthorhombic p form) |
|
56
|
223
|
5t3hA |
Bovine trypsin soaked with selenourea for 5 min |
|
27
|
217
|
5t1vA |
Crystal structure of zika virus ns2b-ns3 protease in apo-form. |
|
50
|
223
|
5ptpA |
Structure of hydrolase (serine proteinase) |
|
58
|
246
|
4zksU |
The crystal structure of upain-1-w3a in complex with inactive upa (upa-s195a) at ph7.4 |
|
41
|
181
|
5c1yA |
Crystal structure of ev71 3c proteinase in complex with compound 1 |
|
59
|
246
|
4zknU |
The crystal structure of upain-1-w3a in complex with upa at ph5.5 |
|
54
|
246
|
4zkrU |
The crystal structure of upain-1-w3a in complex with upa at ph9.0 |
|
88
|
300
|
5c5oA |
Structure of sars-3cl protease complex with a phenyl-beta-alanyl (s,r)-n-decalin type inhibitor |
|
41
|
230
|
5kgoA |
Structure of k. pneumonia mrkh-c-di-gmp complex |
|
44
|
182
|
5iytA |
Complex structure of ev-b93 main protease 3c with n-ethyl 4-((1-cycloheptyl-1,2-dihydropyrazol-3-one-5-yl)-amino)-4-oxo-2z-butenamide |
|
59
|
234
|
4zh8A |
Factor xa complex with gtc000006 |
|
57
|
247
|
4zhmU |
The crystal structure of mupain-1--16-ig in complex with murinised human upa at ph7.4 |
|
60
|
234
|
4zhaA |
Factor xa complex with gtc000102 |
|
52
|
235
|
5jbbS |
Crystal structure of factor ixa variant v16i k98t y177t i213v in complex with egr-chloromethylketone |
|
37
|
180
|
5bpeA |
Crystal structure of ev71 3cpro in complex with a potent and selective inhibitor |
|
58
|
254
|
4zxxH |
Factor viia in complex with the inhibitor n-{3-[(2r)-1-{(2r)-2-[(1-aminoisoquinolin-6-yl)amino]-2-phenylacetyl}pyrrolidin-2-yl]-4-(propan-2-ylsulfonyl)phenyl}acetamide |
|
17
|
99
|
5hiyA |
Crystal structure of pedv nsp9 mutant-c59a |
|
27
|
155
|
5h4iB |
Unlinked ns2b-ns3 protease from zika virus in complex with a compound fragment |
|
40
|
201
|
5hm2A |
Crystal structure of the 3c protease from south african territories type 2 foot-and-mouth disease virus |
|
59
|
246
|
5hggA |
Crystal structure of upa in complex with a camelid-derived antibody fragment |
