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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