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3BEJ

Structure of human FXR in complex with MFA-1 and co-activator peptide

3BEJ の概要
エントリーDOI10.2210/pdb3bej/pdb
分子名称Bile acid receptor, Nuclear receptor coactivator 1, YTTRIUM (III) ION, ... (5 entities in total)
機能のキーワードfxr, bar, nr1h4, bile acid receptor, nhr, nuclear receptor, activator, alternative splicing, dna-binding, metal-binding, nucleus, repressor, transcription, transcription regulation, zinc, zinc-finger, acyltransferase, chromosomal rearrangement, phosphoprotein, polymorphism, proto-oncogene, transferase, ubl conjugation, transcription-transferase complex, transcription regulator
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数4
化学式量合計62313.21
構造登録者
Soisson, S.M.,Parthasarathy, G.,Becker, J.W. (登録日: 2007-11-19, 公開日: 2008-03-18, 最終更新日: 2024-02-21)
主引用文献Soisson, S.M.,Parthasarathy, G.,Adams, A.D.,Sahoo, S.,Sitlani, A.,Sparrow, C.,Cui, J.,Becker, J.W.
Identification of a potent synthetic FXR agonist with an unexpected mode of binding and activation.
Proc.Natl.Acad.Sci.Usa, 105:5337-5342, 2008
Cited by
PubMed: 18391212
DOI: 10.1073/pnas.0710981105
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 3bej
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2024-07-17に公開中

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