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3LZB

EGFR kinase domain complexed with an imidazo[2,1-b]thiazole inhibitor

3LZB の概要
エントリーDOI10.2210/pdb3lzb/pdb
分子名称Epidermal growth factor receptor, N-[3-(5-{2-[(4-morpholin-4-ylphenyl)amino]pyrimidin-4-yl}imidazo[2,1-b][1,3]thiazol-6-yl)phenyl]-2-phenylacetamide (3 entities in total)
機能のキーワードepidermal growth factor kinase domain, multitargeted small molecule kinase inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
由来する生物種Homo sapiens (human)
細胞内の位置Cell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P00533
タンパク質・核酸の鎖数8
化学式量合計291450.65
構造登録者
Swinger, K.K. (登録日: 2010-03-01, 公開日: 2011-03-02, 最終更新日: 2023-09-06)
主引用文献Fidanze, S.D.,Erickson, S.A.,Wang, G.T.,Mantei, R.,Clark, R.F.,Sorensen, B.K.,Bamaung, N.Y.,Kovar, P.,Johnson, E.F.,Swinger, K.K.,Stewart, K.D.,Zhang, Q.,Tucker, L.A.,Pappano, W.N.,Wilsbacher, J.L.,Wang, J.,Sheppard, G.S.,Bell, R.L.,Davidsen, S.K.,Hubbard, R.D.
Imidazo[2,1-b]thiazoles: multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases.
Bioorg.Med.Chem.Lett., 20:2452-2455, 2010
Cited by
PubMed: 20346655
DOI: 10.1016/j.bmcl.2010.03.015
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.7 Å)
構造検証レポート
Validation report summary of 3lzb
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2024-05-01に公開中

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