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3D structures from the PDB for "HIV-1 Protease Mutant V6(46/54/84)" AND "BDBM517"
(Proteins have >= 85% sequence identity and ligands are exact matches)


Seq IdentityJmol DisplayPDB Title
1SGU98%JmolComparing the Accumulation of Active Site and Non-active Site Mutations in the HIV-1 Protease
2B7Z98%JmolStructure of HIV-1 protease mutant bound to indinavir
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
2BPX88%JmolHIV-1 PROTEASE-INHIBITOR COMPLEX
1K6C87%JmolLACK OF SYNERGY FOR INHIBITORS TARGETING A MULTI-DRUG RESISTANT HIV-1 PROTEASE
1SDV86%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1SDU86%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1SDT85%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.