|
60
|
223
|
3fp6E |
Anionic trypsin in complex with bovine pancreatic trypsin inhibitor (bpti) determined to the 1.49 a resolution limit |
|
58
|
234
|
3ffgA |
Factor xa in complex with the inhibitor (r)-6-(2'-((3- hydroxypyrrolidin-1-yl)methyl)biphenyl-4-yl)-1-(3-(5-oxo-4,5-dihydro-1h-1,2,4-triazol-3-yl)phenyl)-3-(trifluoromethyl)-5,6-dihydro-1h-pyrazolo[3,4-c]pyridin- 7(4h)-one |
|
77
|
299
|
3f9hA |
Crystal structure of the f140a mutant of sars-coronovirus 3c-like protease at ph 7.6 |
|
82
|
299
|
3f9fA |
Crystal structure of the f140a mutant of sars-coronovirus 3c-like protease at ph 6.0 |
|
60
|
223
|
3fp8E |
Anionic trypsin variant s195a in complex with bovine pancreatic trypsin inhibitor (bpti) determined to the 1.46 a resolution limit |
|
57
|
258
|
3f68H |
Thrombin inhibition |
|
63
|
223
|
3fp7E |
Anionic trypsin variant s195a in complex with bovine pancreatic trypsin inhibitor (bpti) cleaved at the scissile bond (lys15-ala16) determined to the 1.46 a resolution limit |
|
43
|
240
|
3f6uH |
Crystal structure of human activated protein c (apc) complexed with ppack |
|
59
|
208
|
3f0pA |
Crystal structure of the mercury-bound form of merb, the organomercurial lyase involved in a bacterial mercury resistance system |
|
64
|
238
|
3ensB |
Crystal structure of human fxa in complex with methyl (2z)-3-[(3-chloro-1h-indol-7-yl)amino]-2-cyano-3-{[(3s)-2-oxo-1-(2-oxo-2-pyrrolidin-1-ylethyl)azepan-3-yl]amino}acrylate |
|
61
|
240
|
3estA |
Structure of native porcine pancreatic elastase at 1.65 angstroms resolution |
|
66
|
275
|
3f1sB |
Crystal structure of protein z complexed with protein z-dependent inhibitor |
|
57
|
208
|
3f2gA |
Crystal structure of merb mutant c160s, the organomercurial lyase involved in a bacterial mercury resistance system |
|
41
|
181
|
3eydA |
Structure of hcv ns3-4a protease with an inhibitor derived from a boronic acid |
|
61
|
208
|
3f2fA |
Crystal structure of the mercury-bound form of merb, the organomercurial lyase involved in a bacterial mercury resistance system |
|
16
|
115
|
3f3bA |
Structure of the phage-like element pbsx protein xkdh from bacillus subtilus. northeast structural genomics consortium target sr352. |
|
62
|
208
|
3f0oA |
Crystal structure of merb, the organomercurial lyase involved in a bacterial mercury resistance system |
|
54
|
255
|
3eq0H |
Thrombin inhibitor |
|
50
|
258
|
3edxB |
Crystal structure of the w215a/e217a mutant of murine thrombin |
|
48
|
257
|
3ee0B |
Crystal structure of the w215a/e217a mutant of human thrombin (space group p2(1)2(1)2(1)) |
|
23
|
110
|
3ee7A |
Crystal structure of sars-cov nsp9 g104e |
|
56
|
254
|
3elaH |
Crystal structure of active site inhibited coagulation factor viia mutant in complex with soluble tissue factor |
|
81
|
302
|
3eajA |
Crystal structure of sars-cov main protease quadruple mutant stif/a with two molecules in one asymmetric unit |
|
80
|
305
|
3ea7A |
Crystal structure of sars-cov main protease triple mutant sti/a in space group p21 |
|
53
|
258
|
3egkH |
Knoble inhibitor |
|
85
|
306
|
3ea8A |
Crystal structure of sars-cov main protease triple mutant sti/a in space group c2 |
|
81
|
301
|
3ea9A |
Crystal structure of sars-cov main protease quadruple mutant stif/a with one molecule in one asymmetric unit |
|
64
|
240
|
3e3tA |
Structure of porcine pancreatic elastase with the magic triangle i3c |
|
56
|
258
|
3duxH |
Understanding thrombin inhibition |
|
29
|
176
|
3e90B |
West nile vi rus ns2b-ns3protease in complexed with inhibitor naph-kkr-h |
|
80
|
305
|
3e91A |
Crystal structure of sars-cov mpro mutant in p21 at ph6.9 |
|
51
|
247
|
3e1xB |
The crystal structure of apo prostasin at 1.7 angstroms resolution |
|
52
|
246
|
3e0pB |
The x-ray structure of human prostasin in complex with a covalent benzoxazole inhibitor |
|
18
|
99
|
3dsgA |
Xc1028 from xanthomonas campestris adopts a pilz domain-like structure yet with trivial c-di-gmp binding activity |
|
47
|
251
|
3e0nB |
The x-ray structure of human prostasin in complex with dffr-chloromethyl ketone inhibitor |
|
12
|
66
|
3dspA |
Crystal structure of apo copper resistance protein copk |
|
57
|
258
|
3dt0H |
Understanding thrombin inhibition |
|
61
|
257
|
3e6pH |
Crystal structure of human meizothrombin desf1 |
|
13
|
66
|
3dsoA |
Crystal structure of cu(i) bound copper resistance protein copk |
|
52
|
223
|
3e8lA |
The crystal structure of the double-headed arrowhead protease inhibitor a in complex with two trypsins |
|
50
|
247
|
3e16B |
X-ray structure of human prostasin in complex with benzoxazole warhead peptidomimic, lysine in p3 |
|
55
|
245
|
3dflA |
Crystal structure of human prostasin complexed to 4-guanidinobenzoic acid |
|
55
|
258
|
3dhkH |
Bisphenylic thrombin inhibitors |
|
56
|
248
|
3dfjA |
Crystal structure of human prostasin |
|
55
|
223
|
3d65E |
Crystal structure of textilinin-1, a kunitz-type serine protease inhibitor from the australian common brown snake venom, in complex with trypsin |
|
77
|
283
|
3dclA |
Crystal structure of tm1086 |
|
67
|
258
|
3da9B |
Crystal structure of thrombin in complex with inhibitor |
|
77
|
302
|
3d23A |
Main protease of hcov-hku1 |
|
65
|
299
|
3d62A |
Development of broad-spectrum halomethyl ketone inhibitors against coronavirus main protease 3clpro |
|
57
|
257
|
3d49H |
Thrombin inhibition |
