|
57
|
259
|
1thsH |
Structures of thrombin complexes with a designed and a natural exosite inhibitor |
|
4
|
26
|
1t4vL |
Crystal structure analysis of a novel oxyguanidine bound to thrombin |
|
2
|
32
|
1sr5B |
Antithrombin-anhydrothrombin-heparin ternary complex structure |
|
55
|
259
|
1tbzH |
Human thrombin with active site n-methyl-d phenylalanyl-n-[5-(aminoiminomethyl)amino]-1-{{benzothiazolyl)carbonyl] butyl]-l-prolinamide trifluroacetate and exosite-hirugen |
|
4
|
26
|
1t4uL |
Crystal structure analysis of a novel oxyguanidine bound to thrombin |
|
3
|
25
|
1tbzL |
Human thrombin with active site n-methyl-d phenylalanyl-n-[5-(aminoiminomethyl)amino]-1-{{benzothiazolyl)carbonyl] butyl]-l-prolinamide trifluroacetate and exosite-hirugen |
|
56
|
257
|
1t4uH |
Crystal structure analysis of a novel oxyguanidine bound to thrombin |
|
63
|
287
|
1ta2A |
Crystal structure of thrombin in complex with compound 1 |
|
42
|
256
|
1sr5C |
Antithrombin-anhydrothrombin-heparin ternary complex structure |
|
3
|
49
|
1tbrJ |
Crystal structure of insect derived double domain kazal inhibitor rhodniin in complex with thrombin |
|
53
|
259
|
1tbrH |
Crystal structure of insect derived double domain kazal inhibitor rhodniin in complex with thrombin |
|
68
|
287
|
1ta6A |
Crystal structure of thrombin in complex with compound 14b |
|
3
|
49
|
1tbqJ |
Crystal structure of insect derived double domain kazal inhibitor rhodniin in complex with thrombin |
|
56
|
259
|
1tbqH |
Crystal structure of insect derived double domain kazal inhibitor rhodniin in complex with thrombin |
|
56
|
259
|
1tb6H |
2.5a crystal structure of the antithrombin-thrombin-heparin ternary complex |
|
60
|
257
|
1t4vH |
Crystal structure analysis of a novel oxyguanidine bound to thrombin |
|
3
|
43
|
1tb6L |
2.5a crystal structure of the antithrombin-thrombin-heparin ternary complex |
|
53
|
258
|
1sgiB |
Crystal structure of the anticoagulant slow form of thrombin |
|
57
|
257
|
1sfqB |
Fast form of thrombin mutant r(77a)a bound to ppack |
|
51
|
257
|
1sg8B |
Crystal structure of the procoagulant fast form of thrombin |
|
58
|
258
|
1sb1H |
Novel non-covalent thrombin inhibitors incorporating p1 4,5,6,7-tetrahydrobenzothiazole arginine side chain mimetics |
|
3
|
29
|
1shhA |
Slow form of thrombin bound with ppack |
|
2
|
32
|
1sgiA |
Crystal structure of the anticoagulant slow form of thrombin |
|
3
|
29
|
1sb1L |
Novel non-covalent thrombin inhibitors incorporating p1 4,5,6,7-tetrahydrobenzothiazole arginine side chain mimetics |
|
3
|
29
|
1sfqA |
Fast form of thrombin mutant r(77a)a bound to ppack |
|
64
|
287
|
1sl3A |
Crystal structue of thrombin in complex with a potent p1 heterocycle-aryl based inhibitor |
|
4
|
27
|
1sg8A |
Crystal structure of the procoagulant fast form of thrombin |
|
55
|
257
|
1shhB |
Slow form of thrombin bound with ppack |
|
19
|
102
|
1riwC |
Thrombin in complex with natural product inhibitor oscillarin |
|
28
|
147
|
1riwB |
Thrombin in complex with natural product inhibitor oscillarin |
|
52
|
259
|
1rd3B |
2.5a structure of anticoagulant thrombin variant e217k |
|
7
|
27
|
1riwA |
Thrombin in complex with natural product inhibitor oscillarin |
|
3
|
33
|
1rd3A |
2.5a structure of anticoagulant thrombin variant e217k |
|
1
|
26
|
1qbvL |
Crystal structure of thrombin complexed with an guanidine-mimetic inhibitor |
|
58
|
259
|
1qhrB |
Novel covalent active site thrombin inhibitors |
|
59
|
259
|
1qj6B |
Novel covalent active site thrombin inhibitors |
|
2
|
36
|
1qj1A |
Novel covalent active site thrombin inhibitors |
|
1
|
36
|
1qhrA |
Novel covalent active site thrombin inhibitors |
|
1
|
36
|
1qj6A |
Novel covalent active site thrombin inhibitors |
|
54
|
257
|
1qurH |
Human alpha-thrombin in complex with bivalent, benzamidine-based synthetic inhibitor |
|
59
|
259
|
1qj7B |
Novel covalent active site thrombin inhibitors |
|
2
|
36
|
1qj7A |
Novel covalent active site thrombin inhibitors |
|
3
|
27
|
1qurL |
Human alpha-thrombin in complex with bivalent, benzamidine-based synthetic inhibitor |
|
57
|
257
|
1qbvH |
Crystal structure of thrombin complexed with an guanidine-mimetic inhibitor |
|
60
|
259
|
1qj1B |
Novel covalent active site thrombin inhibitors |
|
2
|
36
|
1ppbL |
The refined 1.9 angstroms crystal structure of human alpha-thrombin: interaction with d-phe-pro-arg chloromethylketone and significance of the tyr-pro-pro-trp insertion segment |
|
55
|
259
|
1ppbH |
The refined 1.9 angstroms crystal structure of human alpha-thrombin: interaction with d-phe-pro-arg chloromethylketone and significance of the tyr-pro-pro-trp insertion segment |
|
7
|
29
|
1p8vB |
Crystal structure of the complex of platelet receptor gpib-alpha and alpha-thrombin at 2.6a |
|
58
|
257
|
1oytH |
Complex of recombinant human thrombin with a designed fluorinated inhibitor |
|
63
|
258
|
1p8vC |
Crystal structure of the complex of platelet receptor gpib-alpha and alpha-thrombin at 2.6a |
