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3BI6

Wee1 kinase complex with inhibitor PD352396

3BI6 の概要
エントリーDOI10.2210/pdb3bi6/pdb
関連するPDBエントリー1x8b 2in6 2io6 2z2w
分子名称Wee1-like protein kinase, CHLORIDE ION, 4-(2-chlorophenyl)-9-hydroxy-6-methyl-1,3-dioxo-N-(2-pyrrolidin-1-ylethyl)pyrrolo[3,4-g]carbazole-8-carboxamide, ... (4 entities in total)
機能のキーワードkinase domain, inhibitor complex, atp-binding, cell cycle, cell division, magnesium, metal-binding, mitosis, nucleotide-binding, nucleus, phosphoprotein, transferase, tyrosine-protein kinase, ubl conjugation
由来する生物種Homo sapiens (human)
細胞内の位置Nucleus: P30291
タンパク質・核酸の鎖数1
化学式量合計32849.20
構造登録者
Squire, C.J.,Dickson, J.M.,Ivanovic, I.,Baker, E.N. (登録日: 2007-11-29, 公開日: 2007-12-18, 最終更新日: 2023-11-01)
主引用文献Smaill, J.B.,Lee, H.H.,Palmer, B.D.,Thompson, A.M.,Squire, C.J.,Baker, E.N.,Booth, R.J.,Kraker, A.,Hook, K.,Denny, W.A.
Synthesis and structure-activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinases.
Bioorg.Med.Chem.Lett., 18:929-933, 2008
Cited by
PubMed: 18191399
DOI: 10.1016/j.bmcl.2007.12.046
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 3bi6
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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