|
58
|
257
|
4uffH |
Thrombin in complex with (2r)-2-(benzylsulfonylamino)-n-(2-((4- carbamimidoylphenyl)methylamino)-2-oxo-ethyl)-n-methyl-3-phenyl- propanamide |
|
37
|
182
|
4u01A |
Hcv ns3/4a serine protease in complex with 6570 |
|
131
|
469
|
4tsfD |
The pathway of binding of the intrinsically disordered mitochondrial inhibitor protein to f1-atpase |
|
57
|
258
|
4uehH |
Thrombin in complex with benzamidine |
|
56
|
258
|
4ud9H |
Thrombin in complex with 5-chlorothiophene-2-carboxamide |
|
54
|
238
|
4ty6A |
Factor xia in complex with the inhibitor 4-{2-[(1s)-1-({[trans-4-(aminomethyl)cyclohexyl]carbonyl}amino)-2-phenylethyl]-1h-imidazol-4-yl}benzamide |
|
57
|
224
|
4u30A |
Human mesotrypsin complexed with bikunin kunitz domain 2 |
|
85
|
306
|
4twyA |
Structure of sars-3cl protease complex with a phenylbenzoyl (s,r)-n-decalin type inhibitor |
|
60
|
223
|
4tpyA |
High throughput screening using acoustic droplet ejection to combine protein crystals and chemical libraries on crystallization plates at high density |
|
57
|
258
|
4udwH |
Thrombin in complex with 1-(2r)-2-amino-3-phenyl-propanoyl-n-(2, 5dichlorophenyl)methylpyrrolidine-2-carboxamide |
|
123
|
469
|
4tt3D |
The pathway of binding of the intrinsically disordered mitochondrial inhibitor protein to f1-atpase |
|
76
|
306
|
4twwA |
Structure of sars-3cl protease complex with a bromobenzoyl (s,r)-n-decalin type inhibitor |
|
55
|
181
|
4sgaE |
Structures of product and inhibitor complexes of streptomyces griseus protease a at 1.8 angstroms resolution. a model for serine protease catalysis |
|
56
|
241
|
4r0iA |
Crystal structure of matriptase in complex with inhibitor |
|
58
|
257
|
4rkoB |
Crystal structure of thrombin mutant s195t bound with ppack |
|
292
|
962
|
4om9A |
X-ray crystal structure of the passenger domain of plasmid encoded toxin, an autrotansporter enterotoxin from enteroaggregative escherichia coli (eaec) |
|
86
|
304
|
4rspA |
X-ray structure of mers-cov nsp5 protease bound with a designed inhibitor |
|
25
|
141
|
4r8tB |
Structure of jev protease |
|
56
|
259
|
4rkjB |
Crystal structure of thrombin mutant s195t (free form) |
|
41
|
243
|
4qt8C |
Crystal structure of ron sema-psi-ipt1 extracellular domains in complex with msp beta-chain |
|
23
|
109
|
4rt0A |
Structure of the alg44 pilz domain from pseudomonas aeruginosa pao1 in complex with c-di-gmp |
|
74
|
325
|
4ri0A |
Serine protease htra3, mutationally inactivated |
|
24
|
108
|
4rt1A |
Structure of the alg44 pilz domain (r95a mutant) from pseudomonas aeruginosa pao1 in complex with c-di-gmp |
|
55
|
290
|
4rn6A |
Structure of prethrombin-2 mutant s195a bound to the active site inhibitor argatroban |
|
52
|
233
|
4q80A |
Neutrophil serine protease 4 (prss57) with val-leu-lys-chloromethylketone (vlk-cmk) |
|
49
|
234
|
4q7yA |
Neutrophil serine protease 4 (prss57) apo form 2 |
|
142
|
459
|
4q4lA |
Crystal structure of an atp synthase subunit beta 1 (f1-b1) from burkholderia thailandensis |
|
259
|
728
|
4p02A |
Structure of bacterial cellulose synthase with cyclic-di-gmp bound. |
|
51
|
245
|
4q2kA |
Bovine alpha chymotrypsin bound to a cyclic peptide inhibitor, 5b |
|
244
|
728
|
4p00A |
Bacterial cellulose synthase in complex with cyclic-di-gmp and udp |
|
54
|
198
|
4proA |
Alpha-lytic protease complexed with pro region |
|
57
|
245
|
4os6A |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk604 (bicyclic 2) |
|
53
|
233
|
4q7zA |
Neutrophil serine protease 4 (prss57) with phe-phe-arg-chloromethylketone (ffr-cmk) |
|
52
|
235
|
4q7xA |
Neutrophil serine protease 4 (prss57) apo form 1 |
|
23
|
93
|
4q63A |
Crystal structure of legionella uncharacterized protein lpg0364 |
|
56
|
237
|
4nffA |
Human kallikrein-related peptidase 2 in complex with ppack |
|
58
|
221
|
4niwA |
Crystal structure of trypsiligase (k60e/n143h/y151h/d189k trypsin) orthorhombic form |
|
40
|
219
|
4o3uA |
Zymogen hgf-beta/met with zymogen activator peptide zap2.3 |
|
51
|
237
|
4nfeA |
Human kallikrein-related peptidase 2 in complex with benzamidine |
|
56
|
245
|
4os5A |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk603 (bicyclic 2) |
|
58
|
241
|
4o9vA |
Crystal structure of matriptase in complex with inhibitor |
|
82
|
264
|
4nsyA |
Wild-type lysobacter enzymogenes lysc endoproteinase covalently inhibited by tlck |
|
60
|
254
|
4ng9H |
Factor viia in complex with the inhibitor (2r)-2-[(1-aminoisoquinolin-6-yl)amino]-2-[3-ethoxy-4-(propan-2-yloxy)phenyl]-n-(3-sulfamoylbenzyl)ethanamide |
|
58
|
245
|
4os2A |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk602 (bicyclic 1) |
|
39
|
219
|
4o3tA |
Zymogen hgf-beta/met with zymogen activator peptide zap.14 |
|
52
|
188
|
4nwkA |
Crystal structure of hepatis c virus protease (ns3) complexed with bms-605339 aka n-(tert-butoxycarbonyl)-3-me thyl-l-valyl-(4r)-n-((1r,2s)-1-((cyclopropylsulfonyl)carba moyl)-2-vinylcyclopropyl)-4-((6-methoxy-1-isoquinolinyl)ox y)-l-prolinamide |
|
57
|
241
|
4o97A |
Crystal structure of matriptase in complex with inhibitor |
|
45
|
218
|
4nzlA |
Extracellular proteins of staphylococcus aureus inhibit the neutrophil serine proteases |
|
51
|
223
|
4niyA |
Crystal structure of trypsiligase (k60e/n143h/y151h/d189k trypsin) complexed to yrh-ecotin (m84y/m85r/a86h ecotin) |
|
52
|
238
|
4na7A |
Factor xia in complex with the inhibitor 3'-[(2s,4r)-6-carbamimidoyl-4-methyl-4-phenyl-1,2,3,4-tetrahydroquinolin-2-yl]-4-carbamoyl-5'-[(3-methylbutanoyl)amino]biphenyl-2-carboxylic acid |
