4L1A
Crystallographic study of multi-drug resistant HIV-1 protease Lopinavir complex: mechanism of drug recognition and resistance
Summary for 4L1A
Entry DOI | 10.2210/pdb4l1a/pdb |
Descriptor | MDR769 HIV-1 protease, N-{1-BENZYL-4-[2-(2,6-DIMETHYL-PHENOXY)-ACETYLAMINO]-3-HYDROXY-5-PHENYL-PENTYL}-3-METHYL-2-(2-OXO-TETRAHYDRO-PYRIMIDIN-1-YL)-BUTYRAMIDE, ... (4 entities in total) |
Functional Keywords | hiv-1 protease, multi-drug resistance, ic50, lopinavir, protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Human immunodeficiency virus 1 (HIV-1) More |
Total number of polymer chains | 2 |
Total formula weight | 22170.04 |
Authors | Liu, Z.,Yedidi, R.S.,Wang, Y.,Dewdney, T.,Reiter, S.,Brunzelle, J.,Kovari, I.,Kovari, L. (deposition date: 2013-06-03, release date: 2014-04-02, Last modification date: 2024-02-28) |
Primary citation | Liu, Z.,Yedidi, R.S.,Wang, Y.,Dewdney, T.G.,Reiter, S.J.,Brunzelle, J.S.,Kovari, I.A.,Kovari, L.C. Crystallographic study of multi-drug resistant HIV-1 protease lopinavir complex: mechanism of drug recognition and resistance. Biochem.Biophys.Res.Commun., 437:199-204, 2013 Cited by PubMed: 23792096DOI: 10.1016/j.bbrc.2013.06.027 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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