|
3
|
28
|
2zffL |
Exploring thrombin s1-pocket |
|
2
|
28
|
2zf0L |
Exploring thrombin s1 pocket |
|
59
|
258
|
2zheH |
Exploring thrombin s3 pocket |
|
3
|
27
|
2zi2L |
Thrombin inhibition |
|
1
|
29
|
2zdaL |
Exploring thrombin s1 pocket |
|
1
|
28
|
2zc9L |
Thrombin in complex with inhibitor |
|
57
|
257
|
2zi2H |
Thrombin inhibition |
|
3
|
27
|
2zgxL |
Thrombin inhibition |
|
59
|
258
|
2zfrH |
Exploring thrombin s3 pocket |
|
56
|
257
|
2zhwH |
Exploring thrombin s3 pocket |
|
3
|
28
|
2zhqL |
Thrombin inhibition |
|
58
|
258
|
2zgbH |
Thrombin inhibition |
|
60
|
258
|
2zhqH |
Thrombin inhibition |
|
1
|
27
|
2zhfL |
Exploring thrombin s3 pocket |
|
59
|
258
|
2zffH |
Exploring thrombin s1-pocket |
|
58
|
258
|
2zc9H |
Thrombin in complex with inhibitor |
|
57
|
258
|
2zgxH |
Thrombin inhibition |
|
58
|
258
|
2zdaH |
Exploring thrombin s1 pocket |
|
58
|
257
|
2zhfH |
Exploring thrombin s3 pocket |
|
55
|
258
|
2zfpH |
Thrombin inibition |
|
1
|
28
|
2zfpL |
Thrombin inibition |
|
57
|
257
|
2v3oH |
Thrombin with 3-cycle with f |
|
2
|
28
|
2v3hL |
Thrombin with 3-cycle no f |
|
2
|
28
|
2v3oL |
Thrombin with 3-cycle with f |
|
59
|
259
|
2uukB |
Thrombin-hirugen-gw420128 ternary complex at 1.39a resolution |
|
60
|
259
|
2uufB |
Thrombin-hirugen binary complex at 1.26a resolution |
|
58
|
257
|
2v3hH |
Thrombin with 3-cycle no f |
|
3
|
28
|
2uufA |
Thrombin-hirugen binary complex at 1.26a resolution |
|
58
|
257
|
2thfB |
Structure of human alpha-thrombin y225f mutant bound to d-phe-pro-arg-chloromethylketone |
|
3
|
28
|
2uujA |
Thrombin-hirugen-gw473178 ternary complex at 1.32a resolution |
|
59
|
259
|
2uujB |
Thrombin-hirugen-gw473178 ternary complex at 1.32a resolution |
|
3
|
28
|
2uukA |
Thrombin-hirugen-gw420128 ternary complex at 1.39a resolution |
|
30
|
145
|
2sptA |
Differences in the metal ion structure between sr-and ca-prothrombin fragment 1 |
|
1
|
26
|
2thfA |
Structure of human alpha-thrombin y225f mutant bound to d-phe-pro-arg-chloromethylketone |
|
5
|
26
|
2r2mA |
2-(2-chloro-6-fluorophenyl)acetamides as potent thrombin inhibitors |
|
64
|
257
|
2r2mB |
2-(2-chloro-6-fluorophenyl)acetamides as potent thrombin inhibitors |
|
2
|
27
|
2pw8L |
Crystal structure of sulfo-hirudin complexed to thrombin |
|
3
|
43
|
2puxA |
Crystal structure of murine thrombin in complex with the extracellular fragment of murine par3 |
|
56
|
258
|
2puxB |
Crystal structure of murine thrombin in complex with the extracellular fragment of murine par3 |
|
55
|
257
|
2pgqB |
Human thrombin mutant c191a-c220a in complex with the inhibitor ppack |
|
22
|
121
|
2pf1A |
Structure of bovine prothrombin fragment 1 refined at 2.25 angstroms resolution |
|
56
|
258
|
2pv9B |
Crystal structure of murine thrombin in complex with the extracellular fragment of murine par4 |
|
3
|
43
|
2pv9A |
Crystal structure of murine thrombin in complex with the extracellular fragment of murine par4 |
|
15
|
102
|
2pksC |
Thrombin in complex with inhibitor |
|
29
|
145
|
2pf2A |
The ca+2 ion and membrane binding structure of the gla domain of ca-prothrombin fragment 1 |
|
58
|
258
|
2pw8H |
Crystal structure of sulfo-hirudin complexed to thrombin |
|
4
|
27
|
2pksA |
Thrombin in complex with inhibitor |
|
26
|
147
|
2pksB |
Thrombin in complex with inhibitor |
|
3
|
35
|
2pgbA |
Inhibitor-free human thrombin mutant c191a-c220a |
|
1
|
43
|
2pgqA |
Human thrombin mutant c191a-c220a in complex with the inhibitor ppack |
