| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
|---|---|---|---|---|---|---|
![]() |
1AB9 | CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN | D | CB |
|
|
![]() |
1LHC | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH | I | H |
|
|
![]() |
1LHD | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROLYS-OH | I | H |
|
|
![]() |
1LHE | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-N-BUTYL-AMIDINO-GLYCINE-OH | I | H |
|
|
![]() |
1LHF | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO-HOMOLYS-OH | I | H |
|
|
![]() |
1LHG | HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROORNITHINE-OH | I | H |
|
|
![]() |
1WBG | ACTIVE SITE THROMBIN INHIBITORS | A | B |
|
|
![]() |
2C8W | THROMBIN INHIBITORS | A | B |
|
|
![]() |
2C8Y | THROMBIN INHIBITORS | A | B |
|
|
![]() |
2C90 | THROMBIN INHIBITORS | A | B |
|
|
![]() |
2JET | CRYSTAL STRUCTURE OF A TRYPSIN-LIKE MUTANT (S189D, A226G) CHYMOTRYPSIN. | A | CB |
|
|
![]() |
2JH0 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
|
|
![]() |
2JH5 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
|
|
![]() |
2JH6 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX. | C | D |
|
|
![]() |
2QL5 | Crystal Structure of caspase-7 with inhibitor AC-DMQD-CHO | G | ABCD |
|
|
![]() |
2QL7 | Crystal Structure of Caspase-7 with inhibitor AC-IEPD-CHO | G | ABCD |
|
|
![]() |
2QL9 | Crystal Structure of Caspase-7 with inhibitor AC-DQMD-CHO | G | ABCD |
|
|
![]() |
2QLB | Crystal Structure of caspase-7 with inhibitor AC-ESMD-CHO | G | ABCD |
|
|
![]() |
2R0L | Short Form HGFA with Inhibitory Fab75 | B | A |
|
|
![]() |
2R2M | 2-(2-Chloro-6-Fluorophenyl)Acetamides as Potent Thrombin Inhibitors | H | B |
|
|
![]() |
2UUF | THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION | A | B |
|
|
![]() |
2UUJ | THROMBIN-HIRUGEN-GW473178 TERNARY COMPLEX AT 1.32A RESOLUTION | A | B |
|
|
![]() |
2UUK | THROMBIN-HIRUGEN-GW420128 TERNARY COMPLEX AT 1.39A RESOLUTION | A | B |
|
|
![]() |
2V3H | THROMBIN WITH 3-CYCLE NO F | I | H |
|
|
![]() |
2V3O | THROMBIN WITH 3-CYCLE WITH F | I | H |
|
|
![]() |
2VU8 | CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN | I | E |
|
|
![]() |
2ZC9 | Thrombin in complex with Inhibitor | L | H |
|
|
![]() |
2ZDA | Exploring Thrombin S1 pocket | L | H |
|
|
![]() |
2ZDV | Exploring Thrombin S1 pocket | L | H |
|
|
![]() |
2ZF0 | Exploring Thrombin S1 Pocket | L | H |
|
|
![]() |
2ZFF | Exploring Thrombin S1-pocket | L | H |
|
|
![]() |
2ZFP | Thrombin Inibition | L | H |
|
|
![]() |
2ZFQ | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZFR | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZG0 | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZGB | Thrombin Inhibition | L | H |
|
|
![]() |
2ZGH | Crystal Structure of active granzyme M bound to its product | B | A |
|
|
![]() |
2ZGJ | Crystal Structure of D86N-GzmM Complexed with Its Optimal Synthesized Substrate | B | A |
|
|
![]() |
2ZGX | Thrombin Inhibition | L | H |
|
|
![]() |
2ZHE | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZHF | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZHQ | Thrombin Inhibition | L | H |
|
|
![]() |
2ZHW | Exploring thrombin S3 pocket | L | H |
|
|
![]() |
2ZI2 | Thrombin Inhibition | L | H |
|
|
![]() |
2ZIQ | Thrombin Inhibition | L | H |
|
|
![]() |
2ZNK | Thrombin Inhibition | L | H |
|
|
![]() |
2ZO3 | Bisphenylic Thrombin Inhibitors | L | H |
|
|
![]() |
3BEF | Crystal structure of thrombin bound to the extracellular fragment of PAR1 | C | B |
|
|
![]() |
3BF6 | Thrombin:suramin complex | L | H |
|
|
![]() |
3BG4 | The crystal structure of guamerin in complex with chymotrypsin and the development of an elastase-specific inhibitor | A | CB |
|