1HVJ
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE
Summary for 1HVJ
Entry DOI | 10.2210/pdb1hvj/pdb |
Descriptor | HIV-1 PROTEASE, N-{1-BENZYL-3-HYDROXY-4-[3-METHYL-2-(3-METHYL-3-PYRIDIN-2-YLMETHYL-UREIDO)-BUTYRYLAMINO]-5-PHENYL-PENTYL}-3-METHYL-2-(3-METHYL-3-PYRIDIN-2-YLMETHYL-UREIDO)-BUTYRAMIDE (3 entities in total) |
Functional Keywords | hydrolase(acid protease) |
Biological source | Human immunodeficiency virus 1 |
Cellular location | Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P04587 |
Total number of polymer chains | 2 |
Total formula weight | 22388.51 |
Authors | Bhat, T.N.,Hosur, M.V.,Baldwin, E.T.,Erickson, J.W. (deposition date: 1994-01-26, release date: 1994-04-30, Last modification date: 2024-02-07) |
Primary citation | Hosur, M.V.,Bhat, T.N.,Kempf, D.,Baldwin, E.T.,Liu, B.,Gulnik, S.,Wideburg, N.E.,Norbeck, D.W.,Appelt, K.,Erickson, J.W. Influence of Stereochemistry on Activity and Binding Modes for C2 Symmetry-Based Diol Inhibitors of HIV-1 Protease J.Am.Chem.Soc., 116:847-855, 1994 Cited by |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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