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2V0M

Crystal structure of human P450 3A4 in complex with ketoconazole

2J0C」から置き換えられました
2V0M の概要
エントリーDOI10.2210/pdb2v0m/pdb
関連するPDBエントリー1TQN 1W0E 1W0F 1W0G 2J0D
分子名称CYTOCHROME P450 3A4, PROTOPORPHYRIN IX CONTAINING FE, 1-ACETYL-4-(4-{[(2S,4R)-2-(2,4-DICHLOROPHENYL)-2-(1H-IMIDAZOL-1-YLMETHYL)-1,3-DIOXOLAN-4-YL]METHOXY}PHENYL)PIPERAZINE (3 entities in total)
機能のキーワードmetal-binding, transmembrane, oxidoreductase, endoplasmic reticulum, drug metabolizing enzyme, ketoconazol, polymorphism, monooxygenase, p450, nadp, iron, heme, cyp3a4, membrane, microsome
由来する生物種HOMO SAPIENS (HUMAN)
タンパク質・核酸の鎖数4
化学式量合計228643.32
構造登録者
Sjogren, T.,Ekroos, M. (登録日: 2007-05-15, 公開日: 2007-06-26, 最終更新日: 2023-12-13)
主引用文献Ekroos, M.,Sjogren, T.
Structural Basis for Ligand Promiscuity in Cytochrome P450 3A4
Proc.Natl.Acad.Sci.USA, 103:13682-, 2006
Cited by
PubMed Abstract: Cytochrome P450 (CYP) 3A4 is the most promiscuous of the human CYP enzymes and contributes to the metabolism of approximately 50% of marketed drugs. It is also the isoform most often involved in unwanted drug-drug interactions. A better understanding of the molecular mechanisms governing CYP3A4-ligand interaction therefore would be of great importance to any drug discovery effort. Here, we present crystal structures of human CYP3A4 in complex with two well characterized drugs: ketoconazole and erythromycin. In contrast to previous reports, the protein undergoes dramatic conformational changes upon ligand binding with an increase in the active site volume by >80%. The structures represent two distinct open conformations of CYP3A4 because ketoconazole and erythromycin induce different types of coordinate shifts. The binding of two molecules of ketoconazole to the CYP3A4 active site and the clear indication of multiple binding modes for erythromycin has implications for the interpretation of the atypical kinetic data often displayed by CYP3A4. The extreme flexibility revealed by the present structures also challenges any attempt to apply computational design tools without the support of relevant experimental data.
PubMed: 16954191
DOI: 10.1073/PNAS.0603236103
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.8 Å)
構造検証レポート
Validation report summary of 2v0m
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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