|
18
|
109
|
1bbrE |
The structure of residues 7-16 of the a alpha chain of human fibrinogen bound to bovine thrombin at 2.3 angstroms resolution |
|
54
|
259
|
1awhB |
Novel covalent thrombin inhibitor from plant extract |
|
3
|
30
|
1ba8A |
Thrombin inhibitor with a rigid tripeptidyl aldehydes |
|
51
|
259
|
1ay6H |
Thrombin inhibitor from theonalla, cyclotheanamide-based macrocyclic tripeptide motif |
|
2
|
36
|
1awhA |
Novel covalent thrombin inhibitor from plant extract |
|
22
|
147
|
1bhxB |
X-ray structure of the complex of human alpha thrombin with the inhibitor sdz 229-357 |
|
53
|
258
|
1b5gH |
Human thrombin complexed with novel synthetic peptide mimetic inhibitor and hirugen |
|
60
|
258
|
1awfH |
Novel covalent thrombin inhibitor from plant extract |
|
55
|
257
|
1bcuH |
Alpha-thrombin complexed with hirugen and proflavin |
|
53
|
256
|
1b7xB |
Structure of human alpha-thrombin y225i mutant bound to d-phe-pro-arg-chloromethylketone |
|
63
|
258
|
1bmmH |
Human alpha-thrombin complexed with [s-(r*,r*)]-4-[(aminoiminomethyl)amino]-n-[[1-[3-hydroxy-2-[(2-naphthalenylsulfonyl)amino]-1-oxopropyl]-2-pyrrolidinyl] methyl]butanamide (bms-186282) |
|
51
|
259
|
1bbrK |
The structure of residues 7-16 of the a alpha chain of human fibrinogen bound to bovine thrombin at 2.3 angstroms resolution |
|
3
|
26
|
1bb0A |
Thrombin inhibitors with rigid tripeptidyl aldehydes |
|
3
|
26
|
1bcuL |
Alpha-thrombin complexed with hirugen and proflavin |
|
1
|
26
|
1b7xA |
Structure of human alpha-thrombin y225i mutant bound to d-phe-pro-arg-chloromethylketone |
|
3
|
41
|
1avgL |
Thrombin inhibitor from triatoma pallidipennis |
|
55
|
257
|
1bmnH |
Human alpha-thrombin complexed with [s-(r*,r*)]-1-(aminoiminomethyl)-n-[[1-[n-[(2-naphthalenylsulfonyl)-l-seryl]-pyrrolidinyl]methyl]-3-piperidenecarboxamide (bms-189090) |
|
20
|
105
|
1bhxF |
X-ray structure of the complex of human alpha thrombin with the inhibitor sdz 229-357 |
|
57
|
258
|
1abjH |
Structure of the hirulog 3-thrombin complex and nature of the s' subsites of substrates and inhibitors |
|
54
|
256
|
1a4wH |
Crystal structures of thrombin with thiazole-containing inhibitors: probes of the s1' binding site |
|
59
|
257
|
1a3eH |
Complex of human alpha-thrombin with the bifunctional boronate inhibitor borolog2 |
|
1
|
36
|
1a2cL |
Structure of thrombin inhibited by aeruginosin298-a from a blue-green alga |
|
61
|
258
|
1ahtH |
Crystal structure of human alpha-thrombin complexed with hirugen and p-amidinophenylpyruvate at 1.6 angstroms resolution |
|
2
|
36
|
1afeL |
Human alpha-thrombin inhibition by cbz-pro-azalys-onp |
|
3
|
27
|
1abjL |
Structure of the hirulog 3-thrombin complex and nature of the s' subsites of substrates and inhibitors |
|
55
|
258
|
1a61H |
Thrombin complexed with a beta-mimetic thiazole-containing inhibitor |
|
1
|
26
|
1a4wL |
Crystal structures of thrombin with thiazole-containing inhibitors: probes of the s1' binding site |
|
50
|
259
|
1a2cH |
Structure of thrombin inhibited by aeruginosin298-a from a blue-green alga |
|
59
|
257
|
1aixH |
Human alpha-thrombin ternary complex with exosite inhibitor hirugen and active site inhibitor phch2oco-d-dpa-pro-boroval |
|
1
|
27
|
1ai8L |
Human alpha-thrombin ternary complex with the exosite inhibitor hirugen and active site inhibitor phch2oco-d-dpa-pro-borompg |
|
3
|
28
|
1ad8L |
Complex of thrombin with and inhibitor containing a novel p1 moiety |
|
56
|
259
|
1abiH |
Structure of the hirulog 3-thrombin complex and nature of the s' subsites of substrates and inhibitors |
|
3
|
27
|
1a5gL |
Human thrombin complexed with novel synthetic peptide mimetic inhibitor and hirugen |
|
56
|
257
|
1a3bH |
Complex of human alpha-thrombin with the bifunctional boronate inhibitor borolog1 |
|
56
|
259
|
1a0hB |
The x-ray crystal structure of ppack-meizothrombin desf1: kringle/thrombin and carbohydrate/kringle/thrombin interactions and location of the linker chain |
|
58
|
257
|
1ai8H |
Human alpha-thrombin ternary complex with the exosite inhibitor hirugen and active site inhibitor phch2oco-d-dpa-pro-borompg |
|
56
|
259
|
1ae8H |
Human alpha-thrombin inhibition by eoc-d-phe-pro-azalys-onp |
|
1
|
33
|
1abiL |
Structure of the hirulog 3-thrombin complex and nature of the s' subsites of substrates and inhibitors |
|
56
|
258
|
1a5gH |
Human thrombin complexed with novel synthetic peptide mimetic inhibitor and hirugen |
|
3
|
26
|
1a46L |
Thrombin complexed with hirugen and a beta-strand mimetic inhibitor |
|
1
|
27
|
1a3bL |
Complex of human alpha-thrombin with the bifunctional boronate inhibitor borolog1 |
|
2
|
27
|
1aixL |
Human alpha-thrombin ternary complex with exosite inhibitor hirugen and active site inhibitor phch2oco-d-dpa-pro-boroval |
|
58
|
259
|
1afeH |
Human alpha-thrombin inhibition by cbz-pro-azalys-onp |
|
58
|
257
|
1ad8H |
Complex of thrombin with and inhibitor containing a novel p1 moiety |
|
3
|
27
|
1a61L |
Thrombin complexed with a beta-mimetic thiazole-containing inhibitor |
|
58
|
258
|
1a46H |
Thrombin complexed with hirugen and a beta-strand mimetic inhibitor |
|
1
|
27
|
1a3eL |
Complex of human alpha-thrombin with the bifunctional boronate inhibitor borolog2 |
|
23
|
159
|
1a0hA |
The x-ray crystal structure of ppack-meizothrombin desf1: kringle/thrombin and carbohydrate/kringle/thrombin interactions and location of the linker chain |
|
3
|
28
|
1ahtL |
Crystal structure of human alpha-thrombin complexed with hirugen and p-amidinophenylpyruvate at 1.6 angstroms resolution |
|
2
|
36
|
1ae8L |
Human alpha-thrombin inhibition by eoc-d-phe-pro-azalys-onp |
