3D structures from the PDB for "HIV-1 protease" AND "BDBM50067593"
(Proteins have >= 85% sequence identity and ligands are exact matches)

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	Seq Identity	Jmol Display	PDB Title
1SGU	0%		COMPARING THE ACCUMULATION OF ACTIVE SITE AND NON-ACTIVE SITE MUTATIONS IN THE HIV-1 PROTEASE 10.1021/BI049459M
1C6Y	0%		ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. 10.1107/S0907444900000469
2BPX	0%		HIV-1 PROTEASE-INHIBITOR COMPLEX 10.1107/S0907444998003588
2AVO	0%		KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S 10.1016/J.JMB.2005.09.095
2AVS	0%		KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S 10.1016/J.JMB.2005.09.095
2AVV	0%		KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S 10.1016/J.JMB.2005.09.095
1K6C	0%		LACK OF SYNERGY FOR INHIBITORS TARGETING A MULTI-DRUG RESISTANT HIV-1 PROTEASE 10.1110/PS.2520102
1HSG	0%		CRYSTAL 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 No DOI
1SDT	0%		CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE. 10.1111/J.1432-1033.2004.04060.X
1SDU	0%		CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE. 10.1111/J.1432-1033.2004.04060.X
1SDV	0%		CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE. 10.1111/J.1432-1033.2004.04060.X
2R5P	0%		CRYSTAL STRUCTURE ANALYSIS OF HIV-1 SUBTYPE C PROTEASE COMPLEXED WITH INDINAVIR 10.1021/BI7018332
2B7Z	0%		STRUCTURE OF HIV-1 PROTEASE MUTANT BOUND TO INDINAVIR No DOI