4QAG
Structure of a dihydroxycoumarin active-site inhibitor in complex with the RNASE H domain of HIV-1 reverse transcriptase
「4JE2」から置き換えられました4QAG の概要
エントリーDOI | 10.2210/pdb4qag/pdb |
関連するPDBエントリー | 3IFJ 3IG1 3K2P 3QLH 4G1Q |
分子名称 | Reverse transcriptase/ribonuclease H, MANGANESE (II) ION, (7,8-dihydroxy-2-oxo-2H-chromen-4-yl)acetic acid, ... (4 entities in total) |
機能のキーワード | rnase h inhibitor, structure-based drug design, active site, transferase, dihydroxycoumarin analogs, dihydroxy-benzopyrone derivatives, divalent cation chelator, aids, reverse transcriptase, protein-inhibitor complex, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
由来する生物種 | Human immunodeficiency virus type 1 (HIV-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 | 30121.44 |
構造登録者 | |
主引用文献 | Himmel, D.M.,Myshakina, N.S.,Ilina, T.,Van Ry, A.,Ho, W.C.,Parniak, M.A.,Arnold, E. Structure of a Dihydroxycoumarin Active-Site Inhibitor in Complex with the RNase H Domain of HIV-1 Reverse Transcriptase and Structure-Activity Analysis of Inhibitor Analogs. J.Mol.Biol., 426:2617-2631, 2014 Cited by PubMed: 24840303DOI: 10.1016/j.jmb.2014.05.006 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.712 Å) |
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