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4I8Z

Crystal structure of wild type HIV-1 protease in complex with non-peptidic inhibitor, GRL008

4I8Z の概要
エントリーDOI10.2210/pdb4i8z/pdb
関連するPDBエントリー4HLA 4I8W
分子名称Protease, (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl [(2S,3R)-4-{[(4-carbamoylphenyl)sulfonyl](2-methylpropyl)amino}-3-hydroxy-1-phenylbutan-2-yl]carbamate (3 entities in total)
機能のキーワードhiv-1 protease, hiv-1 protease-inhibitor complex, hydrolase, grl008, non-peptidic inhibitor, protease inhibitor, 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): P0C6F2
タンパク質・核酸の鎖数2
化学式量合計22183.19
構造登録者
Yedidi, R.S.,Palmer, I.,Das, D.,Wingfield, P.T.,Ghosh, A.K.,Mitsuya, H. (登録日: 2012-12-04, 公開日: 2013-07-24, 最終更新日: 2024-02-28)
主引用文献Yedidi, R.S.,Maeda, K.,Fyvie, W.S.,Steffey, M.,Davis, D.A.,Palmer, I.,Aoki, M.,Kaufman, J.D.,Stahl, S.J.,Garimella, H.,Das, D.,Wingfield, P.T.,Ghosh, A.K.,Mitsuya, H.
P2' benzene carboxylic acid moiety is associated with decrease in cellular uptake: evaluation of novel non-peptidic HIV-1 protease inhibitors containing P2 bis-tetrahydrofuran moiety.
Antimicrob.Agents Chemother., 57:4920-4927, 2013
Cited by
PubMed: 23877703
DOI: 10.1128/AAC.00868-13
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.75 Å)
構造検証レポート
Validation report summary of 4i8z
検証レポート(詳細版)ダウンロードをダウンロード

222415

件を2024-07-10に公開中

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