|
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 |
|
58
|
245
|
4os7A |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk607 (bicyclic) |
|
57
|
236
|
4ogxA |
Crystal structure of fab dx-2930 in complex with human plasma kallikrein at 2.4 angstrom resolution |
|
125
|
524
|
4nzqA |
Crystal structure of ca2+-free prothrombin deletion mutant residues 146-167 |
|
83
|
264
|
4nsvA |
Lysobacter enzymogenes lysc endoproteinase k30r mutant covalently inhibited by tlck |
|
49
|
238
|
4na8A |
Factor xia in complex with the inhibitor 5-aminocarbonyl-2-[3-[(2s,4r)-6-carbamimidoyl-4-methyl-4-phenyl-2,3-dihydro-1h-quinolin-2-yl]phenyl]benzoic acid |
|
56
|
245
|
4os1A |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk601 (bicyclic 1) |
|
50
|
194
|
4nwlA |
Crystal structure of hepatis c virus protease (ns3) complexed with bms-650032 aka n-(tert-butoxycarbonyl)-3-me thyl-l-valyl-(4r)-4-((7-chloro-4-methoxy-1-isoquinolinyl)o xy)-n-((1r,2s)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylc yclopropyl)-l-prolinamide |
|
53
|
219
|
4nivA |
Crystal structure of trypsiligase (k60e/n143h/y151h/d189k trypsin) trigonal form |
|
60
|
254
|
4na9H |
Factor viia in complex with the inhibitor 3'-amino-5'-[(2s,4r)-6-carbamimidoyl-4-phenyl-1,2,3,4-tetrahydroquinolin-2-yl]biphenyl-2-carboxylic acid |
|
118
|
557
|
4o03A |
Crystal structure of ca2+ bound prothrombin deletion mutant residues 146-167 |
|
58
|
223
|
4ncyA |
In situ trypsin crystallized on a mitegen micromesh with imidazole ligand |
|
58
|
239
|
4ogyA |
Crystal structure of fab dx-2930 in complex with human plasma kallikrein at 2.1 angstrom resolution |
|
59
|
221
|
4nixA |
Crystal structure of trypsiligase (k60e/n143h/y151h/d189k trypsin) orthorhombic form, zinc-bound |
|
59
|
254
|
4ngaH |
Factor viia in complex with the inhibitor (2r)-2-[(1-aminoisoquinolin-6-yl)amino]-2-[3-ethoxy-4-(propan-2-yloxy)phenyl]-n-[2-(propan-2-ylsulfonyl)benzyl]ethanamide |
|
56
|
200
|
4mvnA |
Crystal structure of the staphylococcal serine protease spla in complex with a specific phosphonate inhibitor |
|
53
|
243
|
4mpwA |
Human beta-tryptase co-crystal structure with [(1,1,3,3-tetramethyldisiloxane-1,3-diyl)di-1-benzofuran-3,5-diyl]bis({4-[3-(aminomethyl)phenyl]piperidin-1-yl}methanone) |
|
57
|
245
|
4mnxA |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk811 |
|
61
|
223
|
4m7gA |
Streptomyces erythraeus trypsin |
|
54
|
243
|
4mqaA |
Human beta-tryptase co-crystal structure with {(1,1,3,3-tetramethyldisiloxane-1,3-diyl)bis[5-(methylsulfanyl)benzene-3,1-diyl]}bis({4-[3-(aminomethyl)phenyl]piperidin-1-yl}methanone) |
|
58
|
245
|
4mnvA |
Crystal structure of bicyclic peptide uk729 bound as an acyl-enzyme intermediate to urokinase-type plasminogen activator (upa) |
|
39
|
142
|
4mg3A |
Crystal structural analysis of 2a protease from coxsackievirus a16 |
|
55
|
223
|
4mtbA |
Bovine trypsin in complex with small molecule inhibitor |
|
52
|
242
|
4mpxA |
Human beta-tryptase co-crystal structure with [(1,1,3,3-tetramethyldisiloxane-1,3-diyl)di-1-benzothiene-4,2-diyl]bis({4-[3-(aminomethyl)phenyl]piperidin-1-yl}methanone) |
|
59
|
259
|
4mlfB |
Crystal structure for the complex of thrombin mutant d102n and hirudin |
|
59
|
257
|
4lxbH |
Crystal structure analysis of thrombin in complex with compound d58 |
|
55
|
243
|
4mpvA |
Human beta-tryptase co-crystal structure with (2r,4s)-n,n'-bis[3-({4-[3-(aminomethyl)phenyl]piperidin-1-yl}carbonyl)phenyl]-4-hydroxy-2-(2-hydroxypropan-2-yl)-5,5-dimethyl-1,3-dioxolane-2,4-dicarboxamide |
|
54
|
245
|
4mnyA |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk903 |
|
44
|
233
|
4m9fA |
Dengue virus ns2b-ns3 protease a125c variant at ph 8.5 |
|
55
|
245
|
4mnwA |
Crystal structure of urokinase-type plasminogen activator (upa) complexed with bicyclic peptide uk749 |
|
53
|
243
|
4mpuA |
Human beta-tryptase co-crystal structure with (6s,8r)-n,n'-bis[3-({4-[3-(aminomethyl)phenyl]piperidin-1-yl}carbonyl)phenyl]-8-hydroxy-6-(1-hydroxycyclobutyl)-5,7-dioxaspiro[3.4]octane-6,8-dicarboxamide |
|
90
|
303
|
4mdsA |
Discovery of n-(benzo[1,2,3]triazol-1-yl)-n-(benzyl)acetamido)phenyl) carboxamides as severe acute respiratory syndrome coronavirus (sars-cov) 3clpro inhibitors: identification of ml300 and non-covalent nanomolar inhibitors with an induced-fit binding |
|
58
|
257
|
4loyH |
Crystal structure analysis of thrombin in complex with compound d57, 5-chlorothiophene-2-carboxylic acid [(s)-2-[2-methyl-3-(2- oxopyrrolidin-1-yl)benzenesulfonylamino]-3-(4-methylpiperazin-1- yl)-3-oxopropyl]amide (sar107375) |
|
56
|
202
|
4k1sA |
Gly-ser-splb protease from staphylococcus aureus at 1.96 a resolution |
|
58
|
223
|
4kelA |
Atomic resolution crystal structure of kallikrein-related peptidase 4 complexed with a modified sfti inhibitor fcqr(n) |
|
54
|
241
|
4jz1A |
Crystal structure of matriptase in complex with inhibitor |
|
89
|
341
|
4lk4A |
Structure of vibrio cholerae vesb protease |
|
80
|
421
|
4kkdA |
The x-ray crystal structure of mannose-binding lectin-associated serine proteinase-3 reveals the structural basis for enzyme inactivity associated with the 3mc syndrome |
|
48
|
226
|
4k69A |
Crystal structure of human chymase in complex with fragment linked benzimidazolone inhibitor: (3s)-3-{3-[(6-bromo-2-oxo-2,3-dihydro-1h-indol-4-yl)methyl]-2-oxo-2,3-dihydro-1h-benzimidazol-1-yl}hexanoic acid |
|
62
|
254
|
4jzdH |
Structure of factor viia in complex with the inhibitor 2-{2-[(4-carbamimidoylphenyl)carbamoyl]-6-methoxypyridin-3-yl}-5-{[(2s)-1-hydroxy-3,3-dimethylbutan-2-yl]carbamoyl}benzoic acid |
|
58
|
223
|
4ktuA |
Bovine trypsin in complex with microviridin j at ph 6.5 |
|
51
|
223
|
4kgaA |
Crystal structure of kallikrein-related peptidase 4 |
|
59
|
206
|
4k1tA |
Gly-ser-splb protease from staphylococcus aureus at 1.60 a resolution |
|
47
|
177
|
4k8bA |
Crystal structure of hcv ns3/4a protease complexed with inhibitor |
|
48
|
226
|
4k5zA |
Crystal structure of human chymase in complex with fragment inhibitor 6-chloro-2,3-dihydro-1h-isoindol-1-one |
|
60
|
223
|
4ktsA |
Bovine trypsin in complex with microviridin j at ph 8.5 |
|
49
|
226
|
4k2yA |
Crystal structure of human chymase in complex with fragment inhibitor 6-chloro-1,3-dihydro-2h-indol-2-one |
|
56
|
241
|
4jziA |
Crystal structure of matriptase in complex with inhibitor". |
|
40
|
175
|
4ktcA |
Ns3/ns4a protease with inhibitor |
|
55
|
223
|
4k8yA |
Atomic resolution crystal structures of kallikrein-related peptidase 4 complexed with sunflower trypsin inhibitor (sfti-1) |
