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3D structures from the PDB for "HIV-1 Protease Mutant (D30N)" AND "BDBM517"
(Proteins have >= 85% sequence identity and ligands are exact matches)


Seq IdentityJmol DisplayPDB Title
1SDT99%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
2AVO98%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, AND G73S
2AVS98%Jmolkinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
2AVV98%JmolKinetics, stability, and structural changes in high resolution crystal structures of HIV-1 protease with drug resistant mutations L24I, I50V, and G73S
1SDV98%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
1SDU98%JmolCrystal structures of HIV protease V82A and L90M mutants reveal changes in indinavir binding site.
2BPX94%JmolHIV-1 PROTEASE-INHIBITOR COMPLEX
1HSG94%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
1K6C91%JmolLACK OF SYNERGY FOR INHIBITORS TARGETING A MULTI-DRUG RESISTANT HIV-1 PROTEASE
2R5P89%JmolCrystal Structure Analysis of HIV-1 Subtype C Protease Complexed with Indinavir