3R0Y
Crystal Structures of Multidrug-resistant HIV-1 Protease in Complex with Mechanism-Based Aspartyl Protease Inhibitors
Summary for 3R0Y
Entry DOI | 10.2210/pdb3r0y/pdb |
Related | 3R0W |
Related PRD ID | PRD_001113 |
Descriptor | Multidrug-resistant clinical isolate 769 HIV-1 Protease, N-[(2S)-1-{[(2S,3S)-3-hydroxy-5-oxo-5-{[(2R)-1-oxo-3-phenyl-1-(prop-2-yn-1-ylamino)propan-2-yl]amino}-1-phenylpentan-2-yl]amino}-3-methyl-1-oxobutan-2-yl]pyridine-2-carboxamide (3 entities in total) |
Functional Keywords | hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Human immunodeficiency virus 1 |
Total number of polymer chains | 2 |
Total formula weight | 22136.97 |
Authors | Yedidi, R.S.,Gupta, D.,Liu, Z.,Brunzelle, J.,Kovari, I.A.,Woster, P.M.,Kovari, L.C. (deposition date: 2011-03-09, release date: 2012-04-04, Last modification date: 2024-02-21) |
Primary citation | Yedidi, R.S.,Liu, Z.,Wang, Y.,Brunzelle, J.S.,Kovari, I.A.,Woster, P.M.,Kovari, L.C.,Gupta, D. Crystal structures of multidrug-resistant HIV-1 protease in complex with two potent anti-malarial compounds. Biochem.Biophys.Res.Commun., 421:413-417, 2012 Cited by PubMed: 22469467DOI: 10.1016/j.bbrc.2012.03.096 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.65 Å) |
Structure validation
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