|
54
|
257
|
7mj5C |
Complex of human thrombin with xc-43 |
|
3
|
35
|
7sr9A |
Human alpha-thrombin with 180- and 220- loops replaced with homologous loops from protein c |
|
55
|
253
|
7sr9B |
Human alpha-thrombin with 180- and 220- loops replaced with homologous loops from protein c |
|
3
|
31
|
7mj5B |
Complex of human thrombin with xc-43 |
|
57
|
257
|
6hsxH |
Thrombin in complex with a d-phe-pro-diaminopyridine derivative |
|
1
|
28
|
6hsxL |
Thrombin in complex with a d-phe-pro-diaminopyridine derivative |
|
48
|
258
|
8aseB |
Crystal structure of thrombin in complex with macrocycle t3 |
|
2
|
28
|
8aseA |
Crystal structure of thrombin in complex with macrocycle t3 |
|
31
|
579
|
7tppE |
Cryo-em structure of human prothrombin:prothrombinase at 4.1 angstrom resolution |
|
3
|
18
|
8bwwA |
Targeting toll-like receptor-driven systemic inflammation by engineering an innate structural fold into drugs |
|
3
|
31
|
8bw5L |
X-ray structure of the complex between human alpha thrombin and the duplex/quadruplex aptamer m08s-1_41mer |
|
58
|
259
|
8bw5H |
X-ray structure of the complex between human alpha thrombin and the duplex/quadruplex aptamer m08s-1_41mer |
|
3
|
27
|
7zkoL |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form delta |
|
54
|
257
|
7zkoH |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form delta |
|
54
|
259
|
7zkmH |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form beta |
|
58
|
257
|
7zklH |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form alpha |
|
3
|
32
|
7zklL |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form alpha |
|
3
|
27
|
7zkmL |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form beta |
|
55
|
259
|
7zknB |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form gamma |
|
1
|
26
|
7zknA |
X-ray structure of the complex between human alpha thrombin and a pseudo-cyclic thrombin binding aptamer (tba-nnp/ddp) - crystal form gamma |
|
2
|
28
|
6z48A |
Crystal structure of thrombin in complex with macrocycle x1ve |
|
58
|
258
|
6z48B |
Crystal structure of thrombin in complex with macrocycle x1ve |
|
64
|
254
|
7phxH |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - acid-stable sulfotyrosine analogue |
|
6
|
29
|
7phxL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - acid-stable sulfotyrosine analogue |
|
59
|
258
|
7ac9H |
Thrombin in complex with d-arginine (j77) |
|
2
|
28
|
7ac9L |
Thrombin in complex with d-arginine (j77) |
|
1
|
28
|
6zgoL |
Thrombin in complex with d-phe-pro-2-chlorofuran derivative (13l) |
|
56
|
259
|
6zgoH |
Thrombin in complex with d-phe-pro-2-chlorofuran derivative (13l) |
|
56
|
257
|
6yn3H |
Thrombin in complex with 4-hydroxybenzamide (j89) |
|
1
|
28
|
6yn3L |
Thrombin in complex with 4-hydroxybenzamide (j89) |
|
2
|
28
|
6ympL |
Thrombin in complex with 3-((5-(tert-butyl)isoxazol-3-yl)methyl)oxetan-3-amine (j54) |
|
58
|
258
|
6ympH |
Thrombin in complex with 3-((5-(tert-butyl)isoxazol-3-yl)methyl)oxetan-3-amine (j54) |
|
1
|
28
|
6yb6L |
Thrombin in complex with d-phe-pro-3-chloro-1,3-dihydroxybenzylamide derivative (13c) |
|
56
|
257
|
6yb6H |
Thrombin in complex with d-phe-pro-3-chloro-1,3-dihydroxybenzylamide derivative (13c) |
|
57
|
258
|
6yhgH |
Thrombin in complex with d-phe-pro-m-methoxybenzylamide derivative (16a) |
|
57
|
257
|
6y9hH |
Thrombin in complex with d-phe-pro-m-trifluoromethylbenzylamide derivative (phe2) |
|
1
|
31
|
6yhgL |
Thrombin in complex with d-phe-pro-m-methoxybenzylamide derivative (16a) |
|
1
|
28
|
6y9hL |
Thrombin in complex with d-phe-pro-m-trifluoromethylbenzylamide derivative (phe2) |
|
64
|
259
|
7a0dHHH |
The crystal structure of bovine thrombin in complex with hirudin (c16u/c28u) at 1.6 angstroms resolution |
|
8
|
35
|
7a0fLLL |
The crystal structure of bovine thrombin in complex with hirudin (c22u/c39u) at 2.7 angstroms resolution |
|
8
|
35
|
7a0dLLL |
The crystal structure of bovine thrombin in complex with hirudin (c16u/c28u) at 1.6 angstroms resolution |
|
66
|
259
|
7a0fHHH |
The crystal structure of bovine thrombin in complex with hirudin (c22u/c39u) at 2.7 angstroms resolution |
|
65
|
259
|
7a0eHHH |
The crystal structure of bovine thrombin in complex with hirudin (c6u/c14u) at 1.9 angstroms resolution |
|
9
|
40
|
7a0eLLL |
The crystal structure of bovine thrombin in complex with hirudin (c6u/c14u) at 1.9 angstroms resolution |
|
2
|
28
|
6y02L |
Thrombin in complex with 13k |
|
56
|
257
|
6y02H |
Thrombin in complex with 13k |
|
1
|
28
|
6t8aL |
Thrombin in complex with diphenyl ((4-carbamimidoylphenyl)((s)-1-((r)-3-cyclohexyl 2-((phenylmethyl)sulfonamido)propanoyl)pyrrolidine-2-carboxamido)methyl)phosphonate (mi-492) |
|
57
|
258
|
6t52H |
Thrombin in complex with a d-phe-pro-imidazole derivative |
|
9
|
31
|
6tkjL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - tetragonal form at 7kev |
|
8
|
36
|
6tkhL |
Tsetse thrombin inhibitor in complex with human alpha-thrombin - orthorhombic form at 7kev |
