1HVK
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE
1HVK の概要
エントリーDOI | 10.2210/pdb1hvk/pdb |
分子名称 | HIV-1 PROTEASE, N-{1-BENZYL-(2S,3S)-2,3-DIHYDROXY-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) |
機能のキーワード | hydrolase(acid protease) |
由来する生物種 | Human immunodeficiency virus 1 |
細胞内の位置 | Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P03366 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 22402.49 |
構造登録者 | Bhat, T.N.,Hosur, M.V.,Baldwin, E.T.,Erickson, J.W. (登録日: 1994-01-26, 公開日: 1994-04-30, 最終更新日: 2024-02-07) |
主引用文献 | 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 |
実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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