|
72
|
206
|
5c17A |
Crystal structure of the mercury-bound form of merb2 |
|
63
|
208
|
5c0uA |
Crystal structure of the copper-bound form of merb mutant d99s |
|
81
|
306
|
5c5nA |
Structure of sars-3cl protease complex with a phenyl-beta-alanyl (r,s)-n-decalin type inhibitor |
|
43
|
181
|
5c20A |
Crystal structure of ev71 3c proteinase in complex with compound 2 |
|
57
|
224
|
5c67A |
Human mesotrypsin in complex with amyloid precursor protein inhibitor variant appi-m17g/i18f/f34v |
|
39
|
181
|
5c1xA |
Crystal structure of ev71 3c proteinase in complex with compound viii |
|
49
|
251
|
5brrE |
Michaelis complex of tpa-s195a:pai-1 |
|
70
|
248
|
5c2zA |
Molecular insights into the specificity of exfoliative toxins from staphylococcus aureus |
|
39
|
181
|
5c1uA |
Crystal structure of ev71 3c proteinase in complex with compound xb |
|
64
|
208
|
5c0tA |
Crystal structure of the mercury-bound form of merb mutant d99s |
|
64
|
335
|
5b6lA |
Structure of deg protease hhoa from synechocystis sp. pcc 6803 |
|
81
|
310
|
5b6oA |
Crystal structure of ms8104 |
|
42
|
218
|
5a8zA |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
42
|
218
|
5abwA |
Neutrophil elastase inhibitors for the treatment of (cardio)pulmonary diseases |
|
41
|
218
|
5a8xA |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
56
|
257
|
5af9H |
Thrombin in complex with 4-methoxy-n-(2-pyridinyl)benzamide |
|
43
|
218
|
5a8yA |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
42
|
218
|
5a0cA |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
58
|
257
|
5a2mH |
Thrombin inhibitor |
|
44
|
218
|
5a09A |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
42
|
218
|
5a0aE |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
43
|
218
|
5a0bA |
Crystal structure of human neutrophil elastase in complex with a dihydropyrimidone inhibitor |
|
12
|
86
|
4zcnA |
Crystal structure of nvpizza2-s16s58 |
|
59
|
247
|
4zkoU |
The crystal structure of upain-1-w3a in complex with upa at ph7.4 |
|
57
|
247
|
4zhlU |
The crystal structure of mupain-1-ig in complex with murinised human upa at ph7.4 |
|
60
|
249
|
4zmaH |
Crystal structure of a fviia-trypsin chimera (st) in complex with soluble tissue factor |
|
63
|
249
|
4z6aH |
Crystal structure of a fviia-trypsin chimera (yt) in complex with soluble tissue factor |
|
121
|
469
|
4z1mD |
Bovine f1-atpase inhibited by three copies of the inhibitor protein if1 crystallised in the presence of thiophosphate. |
|
60
|
240
|
4ym9A |
Crystal structure of porcine pancreatic elastase (ppe) in complex with the novel inhibitor jm102 |
|
139
|
467
|
4yxwD |
Bovine heart mitochondrial f1-atpase inhibited by amp-pnp and adp in the presence of thiophosphate. |
|
88
|
306
|
4yojA |
Hku4 3clpro bound to non-covalent inhibitor 2a |
|
61
|
254
|
4yt7H |
Factor viia in complex with the inhibitor 2-(2-{(r)-[(4-carbamimidoylphenyl)amino][5-ethoxy-2-fluoro-3-(propan-2-yloxy)phenyl]methyl}-1h-imidazol-4-yl)benzamide |
|
29
|
154
|
4uonA |
Crystal structure of c-terminal truncated (110-265) aura virus capsid protease. |
|
37
|
128
|
4f55A |
Crystal structure of the catalytic domain of the bacillus cereus sleb protein |
|
21
|
99
|
4f48B |
The x-ray structural of fimxeal-c-di-gmp-pilz complexes from xanthomonas campestris |
|
68
|
314
|
4f4oC |
Structure of the haptoglobin-haemoglobin complex |
|
197
|
789
|
4durA |
The x-ray crystal structure of full-length type ii human plasminogen |
|
59
|
240
|
4estE |
Crystal structure of the covalent complex formed by a peptidyl alpha,alpha-difluoro-beta-keto amide with porcine pancreatic elastase at 1.78-angstroms resolution |
|
64
|
259
|
4e05H |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
57
|
258
|
4dt7B |
Crystal structure of thrombin bound to the activation domain qedqvdprlidgkmtrrgds of protein c |
|
56
|
246
|
4dvaU |
The crystal structure of human urokinase-type plasminogen activator catalytic domain |
|
60
|
238
|
4e7nA |
Crystal structure of ahv_tl-i, a glycosylated snake-venom thrombin-like enzyme from agkistrodon halys |
|
54
|
258
|
4dy7B |
Crystal structures of protease nexin-1 in complex with s195a thrombin |
|
38
|
241
|
4dw2U |
The crystal structure of upa in complex with the fab fragment of mab-112 |
|
57
|
257
|
4e7rG |
Thrombin in complex with 3-amidinophenylalanine inhibitor |
|
52
|
223
|
4doqA |
Crystal structure of the complex of porcine pancreatic trypsin with 1/2slpi |
|
60
|
259
|
4e06H |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
28
|
160
|
4dt4A |
Crystal structure of the ppiase-chaperone slpa with the chaperone binding site occupied by the linker of the purification tag |
|
44
|
251
|
4djzB |
Catalytic fragment of masp-1 in complex with its specific inhibitor developed by directed evolution on sgci scaffold |
|
59
|
228
|
4d9rA |
Inhibiting alternative pathway complement activation by targeting the exosite on factor d |
