7LTZ

Bruton's tyrosine kinase in complex with compound 51

7LTZ の概要

• エントリーDOI: 10.2210/pdb7ltz/pdb
• 関連するPDBエントリー: 6W07 7LTY
• 分子名称: Isoform BTK-C of Tyrosine-protein kinase BTK, 1-~{tert}-butyl-~{N}-[(5~{R})-8-[2-[(1-methylpyrazol-4-yl)amino]pyrimidin-4-yl]-2-(oxetan-3-yl)-1,3,4,5-tetrahydro-2-benzazepin-5-yl]-1,2,3-triazole-4-carboxamide, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... (5 entities in total)
• 機能のキーワード: transferase, transferase inhibitor, kinase, kinase inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 32022.83

構造登録者

Metrick, C.M.,Marcotte, D.J. (登録日: 2021-02-20, 公開日: 2022-01-12, 最終更新日: 2023-10-18)

• 主引用文献: Hopkins, B.T.,Bame, E.,Bajrami, B.,Black, C.,Bohnert, T.,Boiselle, C.,Burdette, D.,Burns, J.C.,Delva, L.,Donaldson, D.,Grater, R.,Gu, C.,Hoemberger, M.,Johnson, J.,Kapadnis, S.,King, K.,Lulla, M.,Ma, B.,Marx, I.,Magee, T.,Meissner, R.,Metrick, C.M.,Mingueneau, M.,Murugan, P.,Otipoby, K.L.,Polack, E.,Poreci, U.,Prince, R.,Roach, A.M.,Rowbottom, C.,Santoro, J.C.,Schroeder, P.,Tang, H.,Tien, E.,Zhang, F.,Lyssikatos, J.; Discovery and Preclinical Characterization of BIIB091, a Reversible, Selective BTK Inhibitor for the Treatment of Multiple Sclerosis.; J.Med.Chem., 65:1206-1224, 2022; PubMed: 34734694; DOI: 10.1021/acs.jmedchem.1c00926

実験手法

X-RAY DIFFRACTION (1.53 Å)