2AID
STRUCTURE OF A NON-PEPTIDE INHIBITOR COMPLEXED WITH HIV-1 PROTEASE: DEVELOPING A CYCLE OF STRUCTURE-BASED DRUG DESIGN
2AID の概要
エントリーDOI | 10.2210/pdb2aid/pdb |
分子名称 | HUMAN IMMUNODEFICIENCY VIRUS PROTEASE, CHLORIDE ION, 4-(4-CHLORO-PHENYL)-1-{3-[2-(4-FLUORO-PHENYL)-[1,3]DITHIOLAN-2-YL]-PROPYL}-PIPERIDIN-4-OL, ... (4 entities in total) |
機能のキーワード | aspartyl protease, hiv, non-peptide inhibitor, drug design |
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): P03369 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 22578.53 |
構造登録者 | Rutenber, E.E.,Fauman, E.B.,Keenan, R.J.,Stroud, R.M. (登録日: 1997-04-17, 公開日: 1997-10-15, 最終更新日: 2024-05-22) |
主引用文献 | Rutenber, E.,Fauman, E.B.,Keenan, R.J.,Fong, S.,Furth, P.S.,Ortiz de Montellano, P.R.,Meng, E.,Kuntz, I.D.,DeCamp, D.L.,Salto, R.,Rose, J.R.,Craik, C.S.,Stroud, R.M. Structure of a non-peptide inhibitor complexed with HIV-1 protease. Developing a cycle of structure-based drug design. J.Biol.Chem., 268:15343-15346, 1993 Cited by PubMed: 8340363主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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