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3D structures from the PDB for "Human immunodeficiency virus type 1 protease" AND "BDBM517"
(Proteins have >= 85% sequence identity and ligands are exact matches)


Seq IdentityJmol DisplayPDB Title
2BPX99%JmolHIV-1 PROTEASE-INHIBITOR COMPLEX
1HSG99%JmolCRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES
1SDT94%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
2AVO93%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, AND G73S
1SDV93%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1SDU93%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1K6C93%JmolLACK OF SYNERGY FOR INHIBITORS TARGETING A MULTI-DRUG RESISTANT HIV-1 PROTEASE
2AVS93%Jmolkinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
2AVV93%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
1SGU89%JmolComparing the Accumulation of Active Site and Non-active Site Mutations in the HIV-1 Protease
2B7Z89%JmolStructure of HIV-1 protease mutant bound to indinavir
2R5P88%JmolCrystal Structure Analysis of HIV-1 Subtype C Protease Complexed with Indinavir