|
8
|
29
|
5l6nL |
Disulfated madanin-thrombin complex |
|
57
|
257
|
5lpdH |
Thrombin in complex with (s)-1-((r)-2-amino-3-cyclohexylpropanoyl)-n-(2-(aminomethyl)-5-chlorobenzyl) pyrrolidine-2-carboxamide |
|
1
|
31
|
5lpdL |
Thrombin in complex with (s)-1-((r)-2-amino-3-cyclohexylpropanoyl)-n-(2-(aminomethyl)-5-chlorobenzyl) pyrrolidine-2-carboxamide |
|
58
|
257
|
5jzyH |
Thrombin in complex with (s)-1-((r)-2-amino-3-cyclohexylpropanoyl)-n-(4-carbamimidoylbenzyl)pyrrolidine-2-carboxamide |
|
56
|
259
|
5jduB |
Crystal structure for human thrombin mutant d189a |
|
3
|
29
|
5jzyL |
Thrombin in complex with (s)-1-((r)-2-amino-3-cyclohexylpropanoyl)-n-(4-carbamimidoylbenzyl)pyrrolidine-2-carboxamide |
|
3
|
30
|
5jduA |
Crystal structure for human thrombin mutant d189a |
|
56
|
258
|
5jfdH |
Thrombin in complex with (s)-n-(2-(aminomethyl)-5-chlorobenzyl)-1-((benzylsulfonyl)-d-arginyl)pyrrolidine-2-carboxamide |
|
1
|
26
|
8kme1 |
Crystal structure of human alpha-thrombin inhibited with sel2770. |
|
55
|
257
|
8kme2 |
Crystal structure of human alpha-thrombin inhibited with sel2770. |
|
52
|
259
|
7kmeH |
Crystal structure of human alpha-thrombin inhibited with sel2711. |
|
3
|
25
|
7kmeL |
Crystal structure of human alpha-thrombin inhibited with sel2711. |
|
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 |
|
5
|
27
|
6cymB |
Reversible covalent direct thrombin inhibitors |
|
67
|
257
|
6cymA |
Reversible covalent direct thrombin inhibitors |
|
67
|
582
|
6c2wA |
Crystal structure of human prothrombin mutant s101c/a470c |
|
80
|
582
|
6bjrA |
Crystal structure of prothrombin mutant s101c/a470c |
|
2
|
18
|
5z5xA |
Hvf18 in complex with lps micelles |
|
1
|
12
|
5z5wA |
Vfr12 in complex with lps micelles |
|
1
|
28
|
5af9L |
Thrombin in complex with 4-methoxy-n-(2-pyridinyl)benzamide |
|
56
|
257
|
5af9H |
Thrombin in complex with 4-methoxy-n-(2-pyridinyl)benzamide |
|
3
|
28
|
5afyL |
Thrombin in complex with 3-chloro-benzamide |
|
58
|
257
|
5a2mH |
Thrombin inhibitor |
|
1
|
29
|
5a2mL |
Thrombin inhibitor |
|
1
|
28
|
4e7rL |
Thrombin in complex with 3-amidinophenylalanine inhibitor |
|
64
|
259
|
4e05H |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
57
|
258
|
4dt7B |
Crystal structure of thrombin bound to the activation domain qedqvdprlidgkmtrrgds of protein c |
|
1
|
45
|
4dy7A |
Crystal structures of protease nexin-1 in complex with s195a thrombin |
|
54
|
258
|
4dy7B |
Crystal structures of protease nexin-1 in complex with s195a thrombin |
|
5
|
28
|
4e06L |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
1
|
32
|
4dt7A |
Crystal structure of thrombin bound to the activation domain qedqvdprlidgkmtrrgds of protein c |
|
8
|
29
|
4e05L |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
57
|
257
|
4e7rG |
Thrombin in complex with 3-amidinophenylalanine inhibitor |
|
60
|
259
|
4e06H |
Anophelin from the malaria vector inhibits thrombin through a novel reverse-binding mechanism |
|
5
|
32
|
4ch2A |
Low-salt crystal structure of a thrombin-gpibalpha peptide complex |
|
4
|
26
|
4ch8A |
High-salt crystal structure of a thrombin-gpibalpha peptide complex |
|
63
|
257
|
4ch8B |
High-salt crystal structure of a thrombin-gpibalpha peptide complex |
|
69
|
258
|
4ch2B |
Low-salt crystal structure of a thrombin-gpibalpha peptide complex |
|
64
|
257
|
4bohA |
Madanins (merops i53) are cleaved by thrombin and factor xa |
|
63
|
256
|
4banB |
Thrombin in complex with inhibitor |
|
59
|
257
|
4ax9H |
Human thrombin complexed with napsagatran, ro0466240 |
|
3
|
27
|
4baqA |
Thrombin in complex with inhibitor |
|
65
|
256
|
4bakB |
Thrombin in complex with inhibitor |
|
5
|
30
|
4ayvA |
Human thrombin - inhibitor complex |
|
7
|
28
|
4bohB |
Madanins (merops i53) are cleaved by thrombin and factor xa |
|
3
|
27
|
4bakA |
Thrombin in complex with inhibitor |
|
4
|
27
|
4baoA |
Thrombin in complex with inhibitor |
