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4D2S

Human TTK in complex with a Dyrk1B inhibitor

4D2S の概要
エントリーDOI10.2210/pdb4d2s/pdb
関連するPDBエントリー4D2R
分子名称DUAL SPECIFICITY PROTEIN KINASE TTK, N-{2-methoxy-4-[(1-methylpiperidin-4-yl)oxy]phenyl}-4-(1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine (3 entities in total)
機能のキーワードtransferase, oncology
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33089.01
構造登録者
主引用文献Kettle, J.G.,Ballard, P.,Bardelle, C.,Cockerill, M.,Colclough, N.,Critchlow, S.E.,Debreczeni, J.E.,Fairley, G.,Fillery, S.,Graham, M.A.,Goodwin, L.,Guichard, S.,Hudson, K.,Ward, R.A.,Whittaker, D.
Discovery and Optimization of a Novel Series of Dyrk1B Kinase Inhibitors to Explore a Mek Resistance Hypothesis.
J.Med.Chem., 58:2834-, 2015
Cited by
PubMed Abstract: Potent and selective inhibitors of Dyrk1B kinase were developed to explore the hypothesis, based on siRNA studies, that Dyrk1B may be a resistance mechanism in cells undergoing a stress response.
PubMed: 25738750
DOI: 10.1021/ACS.JMEDCHEM.5B00098
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.5 Å)
構造検証レポート
Validation report summary of 4d2s
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2026-06-24に公開中

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