|
59
|
240
|
2focA |
Structure of porcine pancreatic elastase in 55% dimethylformamide |
|
26
|
150
|
2fomB |
Dengue virus ns2b/ns3 protease |
|
50
|
243
|
2fs8A |
Human beta-tryptase ii with inhibitor cra-29382 |
|
61
|
240
|
2fobA |
Structure of porcine pancreatic elastase in 40/50/10 cyclohexane |
|
61
|
240
|
2foaA |
Structure of porcine pancreatic elastase in 40/50/10 % benzene |
|
60
|
240
|
2fogA |
Structure of porcine pancreatic elastase in 40% trifluoroethanol |
|
59
|
240
|
2fodA |
Structure of porcine pancreatic elastase in 80% ethanol |
|
61
|
223
|
2g55A |
Anomalous substructure of trypsin (p3121) |
|
29
|
152
|
2fp7B |
West nile virus ns2b/ns3protease in complex with bz-nle-lys-arg-arg-h |
|
60
|
234
|
2fzzA |
Factor xa in complex with the inhibitor 1-(3-amino-1,2-benzisoxazol-5-yl)-6-(2'-(((3r)-3-hydroxy-1-pyrrolidinyl)methyl)-4-biphenylyl)-3-(trifluoromethyl)-1,4,5,6-tetrahydro-7h-pyrazolo[3,4-c]pyridin-7-one |
|
48
|
243
|
2fs9A |
Human beta tryptase ii with inhibitor cra-28427 |
|
50
|
243
|
2f9pA |
Crystal structure of the recombinant human alpha i tryptase mutant d216g in complex with leupeptin |
|
59
|
222
|
2fmjA |
220-loop mutant of streptomyces griseus trypsin |
|
59
|
223
|
2fi3E |
Crystal structure of a bpti variant (cys14->ser, cys38->ser) in complex with trypsin |
|
49
|
243
|
2fwwA |
Human beta-tryptase ii complexed with 4-piperidinebutyrate to make acylenzyme |
|
50
|
243
|
2fpzA |
Human tryptase with 2-amino benzimidazole |
|
59
|
240
|
2fofA |
Structure of porcine pancreatic elastase in 80% isopropanol |
|
53
|
242
|
2f9oA |
Crystal structure of the recombinant human alpha i tryptase mutant d216g |
|
58
|
223
|
2ftlE |
Crystal structure of trypsin complexed with bpti at 100k |
|
61
|
240
|
2foeA |
Structure of porcine pancreatic elastase in 80% hexane |
|
42
|
181
|
2fm2A |
Hcv ns3-4a protease domain complexed with a ketoamide inhibitor, sch446211 |
|
59
|
223
|
2fi5E |
Crystal structure of a bpti variant (cys38->ser) in complex with trypsin |
|
135
|
603
|
2f83A |
Crystal structure at 2.9 angstroms resolution of human plasma coagulation factor xi zymogen |
|
56
|
223
|
2ftmA |
Crystal structure of trypsin complexed with the bpti variant (tyr35->gly) |
|
59
|
240
|
2fohA |
Structure of porcine pancreatic elastase in 40% trifluoroethanol |
|
60
|
240
|
2fo9A |
Structure of porcine pancreatic elastase in 95% acetone |
|
59
|
254
|
2flrH |
Novel 5-azaindole factor viia inhibitors |
|
59
|
223
|
2fi4E |
Crystal structure of a bpti variant (cys14->ser) in complex with trypsin |
|
58
|
254
|
2f9bH |
Discovery of novel heterocyclic factor viia inhibitors |
|
51
|
257
|
2feqH |
Orally active thrombin inhibitors |
|
41
|
183
|
2f9uA |
Hcv ns3 protease domain with ns4a peptide and a ketoamide inhibitor with a p2 norborane |
|
65
|
283
|
2f4lA |
Crystal structure of a putative acetamidase (tm0119) from thermotoga maritima msb8 at 2.50 a resolution |
|
55
|
254
|
2flbH |
Discovery of a novel hydroxy pyrazole based factor ixa inhibitor |
|
50
|
237
|
2fdaA |
Crystal structure of the catalytic domain of human coagulation factor xia in complex with alpha-ketothiazole arginine derived ligand |
|
55
|
223
|
2f3cE |
Crystal structure of infestin 1, a kazal-type serineprotease inhibitor, in complex with trypsin |
|
58
|
254
|
2firH |
Crystal structure of dfpr-viia/stf |
|
54
|
257
|
2fesH |
Orally active thrombin inhibitors |
|
11
|
103
|
2eqnA |
Solution structure of the naf1 domain of hypothetical protein bc008207 [homo sapiens] |
|
7
|
73
|
2ey4C |
Crystal structure of a cbf5-nop10-gar1 complex |
|
58
|
233
|
2ei6A |
Factor xa in complex with the inhibitor (-)-cis-n1-[(5-chloroindol-2-yl)carbonyl]-n2-[(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine |
|
58
|
237
|
2f91A |
1.2a resolution structure of a crayfish trypsin complexed with a peptide inhibitor, sgti |
|
60
|
240
|
2estE |
Crystallographic study of the binding of a trifluoroacetyl dipeptide anilide inhibitor with elastase |
|
43
|
183
|
2f9vA |
Hcv ns3 protease domain with ns4a peptide and a ketoamide inhibitor with p1 and p2 cyclopropylalannines |
|
56
|
243
|
2f9nA |
Crystal structure of the recombinant human alpha i tryptase mutant k192q/d216g in complex with leupeptin |
|
104
|
477
|
2f43B |
Rat liver f1-atpase |
|
63
|
233
|
2ei8A |
Factor xa in complex with the inhibitor (1s,2r,4s)-n1-[(5-chloroindol-2-yl)carbonyl]-4-(n,n-dimethylcarbamoyl)-n2-[(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine |
|
44
|
183
|
2ea3A |
Crystal structure of cellulomonas bogoriensis chymotrypsin |
|
60
|
233
|
2ei7A |
Factor xa in complex with the inhibitor trans-n1-[(5-chloroindol-2-yl)carbonyl]-n2-[(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine |
|
57
|
254
|
2ec9H |
Crystal structure analysis of human factor viia , souluble tissue factor complexed with bcx-3607 |
|
48
|
220
|
2eekA |
Crystal structure of atlantic cod trypsin complexed with benzamidine |
