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6GQQ

Crystal structure of human KDR (VEGFR2) kinase domain in complex with AZD3229-analogue (compound 35)

6GQQ の概要
エントリーDOI10.2210/pdb6gqq/pdb
分子名称Vascular endothelial growth factor receptor 2, ~{N}-[4-(6,7-dimethoxyquinazolin-4-yl)oxyphenyl]-2-(4-propan-2-yl-1,2,3-triazol-1-yl)ethanamide (3 entities in total)
機能のキーワードreceptor tyrosine kinase, inhibitor, oncology, gastrointestinal stromal tumour, structure-based drug design, signaling protein
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数1
化学式量合計37438.08
構造登録者
主引用文献Kettle, J.G.,Anjum, R.,Barry, E.,Bhavsar, D.,Brown, C.,Boyd, S.,Campbell, A.,Goldberg, K.,Grondine, M.,Guichard, S.,Hardy, C.J.,Hunt, T.,Jones, R.D.O.,Li, X.,Moleva, O.,Ogg, D.,Overman, R.C.,Packer, M.J.,Pearson, S.,Schimpl, M.,Shao, W.,Smith, A.,Smith, J.M.,Stead, D.,Stokes, S.,Tucker, M.,Ye, Y.
Discovery of N-(4-{[5-Fluoro-7-(2-methoxyethoxy)quinazolin-4-yl]amino}phenyl)-2-[4-(propan-2-yl)-1 H-1,2,3-triazol-1-yl]acetamide (AZD3229), a Potent Pan-KIT Mutant Inhibitor for the Treatment of Gastrointestinal Stromal Tumors.
J. Med. Chem., 61:8797-8810, 2018
Cited by
PubMed: 30204441
DOI: 10.1021/acs.jmedchem.8b00938
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.52 Å)
構造検証レポート
Validation report summary of 6gqq
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2024-07-10に公開中

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