|
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 |
|
58
|
201
|
4inlA |
Crystal structure of spld protease from staphylococcus aureus at 2.1 a resolution |
|
62
|
223
|
4i8lA |
Bovine trypsin at 0.87 resolution |
|
19
|
102
|
4i86A |
Crystal structure of pilz domain of cesa from cellulose synthesizing bacterium |
|
54
|
245
|
4jk5A |
Human urokinase-type plasminogen activator (upa) in complex with a bicyclic peptide inhibitor (uk18-d-ser) |
|
54
|
241
|
4isnA |
Crystal structure of matriptase in complex with its inhibitor hai-1 |
|
41
|
183
|
4imqA |
Structural basis of substrate specificity and protease inhibition in norwalk virus |
|
78
|
393
|
4j1yA |
The x-ray crystal structure of human complement protease c1s zymogen |
|
63
|
223
|
4i8kA |
Bovine trypsin at 0.85 resolution |
|
62
|
254
|
4jzeH |
Structure of factor viia in complex with the inhibitor 2-{2-[(1-aminoisoquinolin-6-yl)carbamoyl]-6-methoxypyridin-3-yl}-5-{[(2s)-1-hydroxy-3,3-dimethylbutan-2-yl]carbamoyl}benzoic acid |
|
46
|
182
|
4i33A |
Crystal structure of hcv ns3/4a r155k protease complexed with compound 4 |
|
55
|
216
|
4jcnA |
Structure of esp, serine protease from staphylococcus epidermidis |
|
85
|
352
|
4ic6A |
Crystal structure of deg8 |
|
57
|
241
|
4jytA |
Crystal structure of matriptase in complex with inhibitor |
|
61
|
223
|
4i8hA |
Bovine trypsin at 0.75 resolution |
|
55
|
245
|
4jk6A |
Human urokinase-type plasminogen activator (upa) in complex with a bicyclic peptide inhibitor (uk18-d-aba) |
|
37
|
182
|
4in1A |
Structural basis of substrate specificity and protease inhibition in norwalk virus |
|
55
|
223
|
4k1eA |
Atomic resolution crystal structures of kallikrein-related peptidase 4 complexed with a modified sfti inhibitor fcqr |
|
61
|
203
|
4inkA |
Crystal structure of spld protease from staphylococcus aureus at 1.56 a resolution |
|
62
|
254
|
4jzfH |
Structure of factor viia in complex with the inhibitor 2-{2-[(3-carbamoylphenyl)carbamoyl]-6-methoxypyridin-3-yl}-5-{[(2s)-1-hydroxy-3,3-dimethylbutan-2-yl]carbamoyl}benzoic acid |
|
58
|
241
|
4is5A |
Crystal structure of the ligand-free inactive matriptase |
|
57
|
254
|
4iblH |
Rubidium sites in blood coagulation factor viia |
|
59
|
254
|
4jyuH |
Structure of factor viia in complex with the inhibitor (2r)-2-[(1-aminoisoquinolin-6-yl)amino]-2-[3-ethoxy-4-(propan-2-yloxy)phenyl]-n-(phenylsulfonyl)ethanamide |
|
62
|
223
|
4i8jA |
Bovine trypsin at 0.87 a resolution |
|
45
|
182
|
4jmyA |
Crystal structure of hcv ns3/ns4a protease complexed with ddivpc peptide |
|
42
|
182
|
4i31A |
Crystal structure of hcv ns3/ns4a protease complexed with compound 4 |
|
59
|
254
|
4ishH |
Structure of factor viia in complex with the inhibitor bms-593214 also known as 2'-[(6r,6ar,11br)-2-carbamimidoyl-6,6a,7,11b-tetrahydro-5h-indeno[2,1-c]quinolin-6-yl]-5'-hydroxy-4'-methoxybiphenyl-4-carboxylic acid |
|
41
|
183
|
4imzA |
Structural basis of substrate specificity and protease inhibition in norwalk virus |
|
78
|
402
|
4igdA |
Crystal structure of the zymogen catalytic region of human masp-1 |
|
56
|
241
|
4islA |
Crystal structure of the inactive matriptase in complex with its inhibitor hai-1 |
|
41
|
178
|
4inhA |
Structural basis of substrate specificity and protease inhibition in norwalk virus |
|
29
|
181
|
4in2A |
Structural basis of substrate specificity and protease inhibition in norwalk virus |
|
79
|
411
|
4hzhA |
Structure of recombinant gla-domainless prothrombin mutant s525a |
|
48
|
274
|
4iw4E |
Crystal structure of the serine protease domain of masp-3 in complex with ecotin |
|
60
|
254
|
4isiH |
Structure of factor viia in complex with the inhibitor (6s)-n-(4-carbamimidoylbenzyl)-1-chloro-3-(cyclobutylamino)-8,8-diethyl-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrazine-6-carboxamide |
|
43
|
237
|
4ic5A |
Crystal structure of deg5 |
|
62
|
223
|
4i8gA |
Bovine trypsin at 0.8 resolution |
|
58
|
254
|
4jyvH |
Structure of factor viia in complex with the inhibitor (2r)-2-[3-ethoxy-4-(propan-2-yloxy)phenyl]-2-(isoquinolin-6-ylamino)-n-[(3-sulfamoylphenyl)sulfonyl]ethanamide |
|
42
|
182
|
4i32A |
Crystal structure of hcv ns3/4a d168v protease complexed with compound 4 |
|
55
|
223
|
4j2yB |
Crystal structure of a plant trypsin inhibitor ecti in complex with bovine trypsin. |
|
57
|
241
|
4isoA |
Crystal structure of matriptase in complex with its inhibitor hai-1 |
|
53
|
257
|
4htcH |
The refined structure of the hirudin-thrombin complex |
|
233
|
747
|
4hg6A |
Structure of a cellulose synthase - cellulose translocation intermediate |
|
51
|
259
|
4h6sB |
Crystal structure of thrombin mutant e14ea/d14la/e18a/s195a |
|
50
|
257
|
4hfpB |
Structure of thrombin mutant s195a bound to the active site inhibitor argatroban |
|
82
|
300
|
4hi3A |
Crystal structure of dimeric r298a mutant of sars coronavirus main protease |
|
54
|
247
|
4h42U |
Synthesis of a weak basic upa inhibitor and crystal structure of complex with upa |
|
60
|
223
|
4hgcA |
Crystal structure of bovine trypsin complexed with sfti-1 analog containing a peptoid residue at position p1 |
