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5P9F

BTK IN COMPLEX WITH GDC-0834

5P9F の概要
エントリーDOI10.2210/pdb5p9f/pdb
Group depositionCrystal structures of Tyrosine-protein kinase BTK in complex with inhibitors (G_1002011)
分子名称Tyrosine-protein kinase BTK, N-{3-[6-({4-[(2R)-1,4-dimethyl-3-oxopiperazin-2-yl]phenyl}amino)-4-methyl-5-oxo-4,5-dihydropyrazin-2-yl]-2-methylphenyl }-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxamide, 1,2-ETHANEDIOL, ... (5 entities in total)
機能のキーワードlead optimization, protein kinase, transferase
由来する生物種Homo sapiens (Human)
細胞内の位置Cytoplasm: Q06187
タンパク質・核酸の鎖数1
化学式量合計33263.18
構造登録者
Gardberg, A.S. (登録日: 2016-09-20, 公開日: 2017-05-24, 最終更新日: 2021-11-17)
主引用文献Bender, A.T.,Gardberg, A.,Pereira, A.,Johnson, T.,Wu, Y.,Grenningloh, R.,Head, J.,Morandi, F.,Haselmayer, P.,Liu-Bujalski, L.
Ability of Bruton's Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling.
Mol. Pharmacol., 91:208-219, 2017
Cited by
PubMed: 28062735
DOI: 10.1124/mol.116.107037
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.71 Å)
構造検証レポート
Validation report summary of 5p9f
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2024-04-24に公開中

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