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3D structures from the PDB for "HIV-1 Protease Mutant Q-60C" AND "BDBM517"
(Proteins have >= 85% sequence identity and ligands are exact matches)


Seq IdentityJmol DisplayPDB Title
1SGU88%JmolComparing the Accumulation of Active Site and Non-active Site Mutations in the HIV-1 Protease
2B7Z88%JmolStructure of HIV-1 protease mutant bound to indinavir
2BPX88%JmolHIV-1 PROTEASE-INHIBITOR COMPLEX
1HSG88%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
1SDU87%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1K6C87%JmolLACK OF SYNERGY FOR INHIBITORS TARGETING A MULTI-DRUG RESISTANT HIV-1 PROTEASE
1SDV87%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1SDT86%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
2AVV85%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
2AVS85%Jmolkinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
2AVO85%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, AND G73S