|
25
|
85
|
6dcmA |
The atomic resolution crystal structure of kringle 2 variant bound with eaca |
|
6
|
85
|
6fwnA |
Structure and dynamics of the platelet integrin-binding c4 domain of von willebrand factor |
|
1
|
28
|
5mm6L |
Thrombin mutant a190s in complex with (s)-1-(d-phenylalanyl)-n-(4-carbamimidoylbenzyl)pyrrolidine-2-carboxamide |
|
58
|
258
|
5mm6H |
Thrombin mutant a190s in complex with (s)-1-(d-phenylalanyl)-n-(4-carbamimidoylbenzyl)pyrrolidine-2-carboxamide |
|
103
|
716
|
5k8dA |
Crystal structure of rfviiifc |
|
90
|
639
|
5k8dB |
Crystal structure of rfviiifc |
|
9
|
57
|
6f1fA |
The methylene thioacetal bpti (bovine pancreatic trypsin inhibitor) mutant structure |
|
58
|
257
|
6eo9H |
Crystal structure of thrombin in complex with a novel glucose-conjugated potent inhibitor |
|
3
|
26
|
6eo8L |
Crystal structure of thrombin in complex with a novel glucose-conjugated potent inhibitor |
|
58
|
256
|
6eo8H |
Crystal structure of thrombin in complex with a novel glucose-conjugated potent inhibitor |
|
2
|
26
|
6eo9L |
Crystal structure of thrombin in complex with a novel glucose-conjugated potent inhibitor |
|
67
|
582
|
6c2wA |
Crystal structure of human prothrombin mutant s101c/a470c |
|
45
|
243
|
6b77B |
Structures of the two-chain human plasma factor xiia co-crystallized with potent inhibitors |
|
50
|
243
|
6b74B |
Structures of the two-chain human plasma factor xiia co-crystallized with potent inhibitors |
|
14
|
40
|
5v4uA |
Solution structure of vkk38 bound to plasminogen kringle 2 |
|
74
|
209
|
5bv8A |
G1324s mutation in von willebrand factor a1 domain |
|
3
|
28
|
5afyL |
Thrombin in complex with 3-chloro-benzamide |
|
118
|
436
|
4eb1I |
Hyperstable in-frame insertion variant of antithrombin |
|
109
|
424
|
4eb1L |
Hyperstable in-frame insertion variant of antithrombin |
|
37
|
326
|
4bxsA |
Crystal structure of the prothrombinase complex from the venom of pseudonaja textilis |
|
69
|
322
|
4bxwA |
Crystal structure of the prothrombinase complex from the venom of pseudonaja textilis |
|
60
|
264
|
4c2bB |
Crystal structure of high-affinity von willebrand factor a1 domain with disulfide mutation in complex with high affinity gpib alpha |
|
70
|
201
|
4c29A |
Crystal structure of high-affinity von willebrand factor a1 domain with disulfide mutation |
|
220
|
1429
|
4bxsV |
Crystal structure of the prothrombinase complex from the venom of pseudonaja textilis |
|
25
|
115
|
4ccvA |
Crystal structure of histidine-rich glycoprotein n2 domain reveals redox activity at an interdomain disulfide bridge: implications for the regulation of angiogenesis |
|
72
|
266
|
4c2aB |
Crystal structure of high-affinity von willebrand factor a1 domain with r1306q and i1309v mutations in complex with high affinity gpib alpha |
|
73
|
202
|
4c2aA |
Crystal structure of high-affinity von willebrand factor a1 domain with r1306q and i1309v mutations in complex with high affinity gpib alpha |
|
58
|
199
|
4c2bA |
Crystal structure of high-affinity von willebrand factor a1 domain with disulfide mutation in complex with high affinity gpib alpha |
|
13
|
78
|
4bqdA |
Kd1 of human tfpi in complex with a synthetic peptide |
|
2
|
20
|
4bqdC |
Kd1 of human tfpi in complex with a synthetic peptide |
|
104
|
640
|
4bdvB |
Crystal structure of a truncated b-domain human factor viii |
|
111
|
713
|
4bdvA |
Crystal structure of a truncated b-domain human factor viii |
|
66
|
181
|
3zqkA |
Von willebrand factor a2 domain with calcium |
|
66
|
345
|
4aqbA |
Mbl-ficolin associated protein-1, map-1 aka map44 |
|
116
|
379
|
4ajtA |
The crystal structure of mouse protein-z dependent protease inhibitor(mzpi) |
|
89
|
352
|
4ajuA |
Crystal structure of the reactive loop cleaved zpi in p41 space group |
|
1
|
36
|
4ajuB |
Crystal structure of the reactive loop cleaved zpi in p41 space group |
|
32
|
174
|
5ou8A |
Crystal structure of glycoprotein vi in complex with collagen-peptide (gpo)5 |
|
31
|
179
|
5ou9A |
Crystal structure of glycoprotein vi in complex with collagen-peptide (gpo)3 |
|
36
|
173
|
5ou7A |
Crystal structure of the glycoprotein vi loop truncation mutant pavs-papykn |
|
0
|
11
|
5mm6I |
Thrombin mutant a190s in complex with (s)-1-(d-phenylalanyl)-n-(4-carbamimidoylbenzyl)pyrrolidine-2-carboxamide |
|
115
|
378
|
5hgcA |
A serpin structure |
|
3
|
70
|
5iecA |
Structural basis for therapeutic inhibition of complement c5 |
|
59
|
257
|
5afyH |
Thrombin in complex with 3-chloro-benzamide |
|
59
|
257
|
5afzH |
Thrombin in complex with (2r)-2-(benzylsulfonylamino)-n-(2-((4- carbamimidoylphenyl)methylamino)-2-oxo-propyl)-3-phenyl-propanamide |
|
1
|
28
|
5afzL |
Thrombin in complex with (2r)-2-(benzylsulfonylamino)-n-(2-((4- carbamimidoylphenyl)methylamino)-2-oxo-propyl)-3-phenyl-propanamide |
|
56
|
241
|
4xdeA |
Coagulation factor xii protease domain crystal structure |
|
46
|
238
|
4xe4A |
Coagulation factor xii protease domain crystal structure |
|
57
|
246
|
4xskU |
Structure of paitrap, an upa mutant |
|
65
|
182
|
4tpvA |
Crystal structure of hookworm platelet inhibitor |
