|
57
|
254
|
2ec9H |
Crystal structure analysis of human factor viia , souluble tissue factor complexed with bcx-3607 |
|
58
|
240
|
2de9A |
Crystal structure of porcine pancreatic elastase complexed with tris after soaking a tris-free solution |
|
48
|
223
|
2d8wA |
Structure of hyper-vil-trypsin |
|
79
|
301
|
2d2dA |
Crystal structure of sars-cov mpro in complex with an inhibitor i2 |
|
32
|
236
|
2d26C |
Active site distortion is sufficient for proteinase inhibit second crystal structure of covalent serpin-proteinase complex |
|
62
|
240
|
2cv3A |
Crystal structure of porcine pancreatic elastase complexed with a macroclyclic peptide inhibitor |
|
57
|
240
|
2de8A |
Crystal structure of porcine pancreatic elastase with a unique conformation induced by tris |
|
53
|
212
|
2cxvA |
Dual modes of modification of hepatitis a virus 3c protease by a serine-derived betalactone: selective crystallization and high-resolution structure of the his-102 adduct |
|
61
|
257
|
2cf8H |
Complex of recombinant human thrombin with an inhibitor |
|
58
|
233
|
2d1jA |
Factor xa in complex with the inhibitor 2-[[4-[(5-chloroindol-2-yl)sulfonyl]piperazin-1-yl] carbonyl]thieno[3,2-b]pyridine n-oxide |
|
58
|
223
|
2cmyA |
Crystal complex between bovine trypsin and veronica hederifolia trypsin inhibitor |
|
156
|
467
|
2ck3D |
Azide inhibited bovine f1-atpase |
|
62
|
259
|
2c8zB |
Thrombin inhibitors |
|
58
|
234
|
2cjiA |
Crystal structure of a human factor xa inhibitor complex |
|
60
|
257
|
2cn0H |
Complex of recombinant human thrombin with a designed inhibitor |
|
55
|
245
|
2cgaA |
Bovine chymotrypsinogen a. x-ray crystal structure analysis and refinement of a new crystal form at 1.8 angstroms resolution |
|
57
|
254
|
2c4fH |
Crystal structure of factor vii.stf complexed with pd0297121 |
|
15
|
97
|
2chaC |
The structure of crystalline alpha-chymotrypsin, $v.the atomic structure of tosyl-alpha-chymotrypsin at 2 angstroms resolution |
|
60
|
259
|
2c8xB |
Thrombin inhibitors |
|
57
|
257
|
2cf9H |
Complex of recombinant human thrombin with an inhibitor |
|
59
|
259
|
2c90B |
Thrombin inhibitors |
|
84
|
301
|
2c3sA |
Structure of sars cov main proteinase at 1.9 a (ph6.5) |
|
14
|
131
|
2chaB |
The structure of crystalline alpha-chymotrypsin, $v.the atomic structure of tosyl-alpha-chymotrypsin at 2 angstroms resolution |
|
55
|
223
|
2by8X |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
55
|
223
|
2by9X |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
58
|
259
|
2c8wB |
Thrombin inhibitors |
|
55
|
223
|
2byaX |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
59
|
259
|
2c8yB |
Thrombin inhibitors |
|
55
|
223
|
2by6X |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
59
|
259
|
2c93B |
Thrombin inhibitors |
|
59
|
257
|
2bxtH |
Design and discovery of novel, potent thrombin inhibitors with a solubilizing cationic p1-p2-linker |
|
54
|
223
|
2by5X |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
53
|
223
|
2by7X |
Is radiation damage dependent on the dose-rate used during macromolecular crystallography data collection |
|
59
|
250
|
2bvrH |
Human thrombin complexed with fragment-based small molecules occupying the s1 pocket |
|
89
|
300
|
2bx3A |
Crystal structure of sars coronavirus main proteinase (p43212) |
|
58
|
257
|
2bxuH |
Design and discovery of novel, potent thrombin inhibitors with a solubilizing cationic p1-p2-linker |
|
60
|
234
|
2bqwB |
Crystal structure of factor xa in complex with compound 45 |
|
46
|
242
|
2bm2A |
Human beta-ii tryptase in complex with 4-(3-aminomethyl-phenyl)- piperidin-1-yl-(5-phenethyl- pyridin-3-yl)-methanone |
|
55
|
254
|
2bz6H |
Orally available factor7a inhibitor |
|
57
|
223
|
2bzaA |
Bovine pancreas beta-trypsin in complex with benzylamine |
|
72
|
298
|
2bx4A |
Crystal structure of sars coronavirus main proteinase (p21212) |
|
58
|
257
|
2bvsH |
Human thrombin complexed with fragment-based small molecules occupying the s1 pocket |
|
61
|
234
|
2bq6B |
Crystal structure of factor xa in complex with 21 |
|
56
|
223
|
2blvA |
Trypsin before a high dose x-ray "burn" |
|
56
|
233
|
2bokA |
Factor xa - cation |
|
63
|
240
|
2blqA |
Elastase after a high dose x-ray "burn" |
|
47
|
223
|
2bdhA |
Human kallikrein 4 complex with zinc and p-aminobenzamidine |
|
46
|
223
|
2bdiA |
Human kallikrein 4 complex with cobalt and p-aminobenzamidine |
|
62
|
240
|
2bd5A |
Porcine pancreatic elastase complexed with beta-casomorphin-7 and lys-ser at ph 5 and immersed in ph 9 buffer for 30 seconds |
|
57
|
254
|
2b7dH |
Factor viia inhibitors: chemical optimization, preclinical pharmacokinetics, pharmacodynamics, and efficacy in a baboon thrombosis model |
