3D structures from the PDB for "Protease" AND "BDBM50488871"
(Proteins have >= 85% sequence identity and ligands are exact matches)

Seq IdentityJmol DisplayPDB Title
3KF095%JmolHIV PROTEASE WITH FRAGMENT 4D9 BOUND
3KFS95%JmolHIV PROTEASE (PR) DIMER WITH INHIBITOR TL-3 BOUND AND FRAGMENT 2F4 IN THE OUTSIDE/TOP OF FLAP
3KFR95%JmolHIV PROTEASE (PR) DIMER WITH INHIBITOR TL-3 BOUND AND FRAGMENT 1F1 IN THE OUTSIDE/TOP OF FLAP
3KFN95%JmolHIV PROTEASE (PR) WITH INHIBITOR TL-3 AND FRAGMENT HIT 4D9 BY SOAKING
5VEA95%JmolHIV PROTEASE (PR) WITH TL-3 IN ACTIVE SITE AND 4-METHYLBENZENE-1,2- DIAMINE IN EXOSITE
2AZ895%JmolHIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3
4TVH95%JmolHIV PROTEASE (PR) DIMER IN CLOSED FORM WITH TL-3 IN ACTIVE SITE AND FRAGMENT AK-2097 IN THE OUTSIDE/TOP OF FLAP
3KFP95%JmolHIV PROTEASE (PR) WITH INHIBITOR TL-3 BOUND, AND DMSOS IN EXO SITE
5VCK95%JmolHIV PROTEASE (PR) WITH TL-3 IN THE ACTIVE SITE AND (Z)-N-(THIAZOL-2- YL)-N'-TOSYLCARBAMIMIDATE IN THE EXOSITE
2AZ994%JmolHIV-1 PROTEASE NL4-3 1X MUTANT
3TLH94%JmolSTRUCTURAL STUDIES OF HIV AND FIV PROTEASES COMPLEXED WITHAN EFFICIENT INHIBITOR OF FIV PR
4K4R94%JmolTL-3 INHIBITED TRP6ALA HIV PROTEASE WITH 1-BROMO-2-NAPTHOIC ACID BOUND IN EXOSITE
4K4Q94%JmolTL-3 INHIBITED TRP6ALA HIV PROTEASE WITH 3-BROMO-2,6-DIMETHOXYBENZOIC ACID BOUND IN FLAP SITE
4K4P94%JmolTL-3 INHIBITED TRP6ALA HIV PROTEASE
2P3B94%JmolCRYSTAL STRUCTURE OF THE SUBTYPE B WILD TYPE HIV PROTEASE COMPLEXED WITH TL-3 INHIBITOR
2AZB92%JmolHIV-1 PROTEASE NL4-3 3X MUTANT IN COMPLEX WITH INHIBITOR, TL-3
5W5W92%JmolHIV PROTEASE (PR) IN OPEN FORM WITH MG2+ IN ACTIVE SITE AND HIVE-9 IN EYE SITE
2AZC90%JmolHIV-1 PROTEASE NL4-3 6X MUTANT