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4YND

The Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2

4YND の概要
エントリーDOI10.2210/pdb4ynd/pdb
分子名称N-lysine methyltransferase SMYD2, ZINC ION, N-cyclohexyl-N~3~-[2-(3,4-dichlorophenyl)ethyl]-N-(2-{[(2R)-2-hydroxy-2-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-8-yl)ethyl]amino}ethyl)-beta-alaninamide, ... (5 entities in total)
機能のキーワードepigenetics, smyd2, h3k36, p53, methyltransferase, lysine, transferase-inhibitor complex, transferase/inhibitor
由来する生物種Homo sapiens (Human)
細胞内の位置Cytoplasm, cytosol : Q9NRG4
タンパク質・核酸の鎖数1
化学式量合計54378.00
構造登録者
主引用文献Sweis, R.F.,Wang, Z.,Algire, M.,Arrowsmith, C.H.,Brown, P.J.,Chiang, G.G.,Guo, J.,Jakob, C.G.,Kennedy, S.,Li, F.,Maag, D.,Shaw, B.,Soni, N.B.,Vedadi, M.,Pappano, W.N.
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2.
Acs Med.Chem.Lett., 6:695-700, 2015
Cited by
PubMed Abstract: A lack of useful small molecule tools has precluded thorough interrogation of the biological function of SMYD2, a lysine methyltransferase with known tumor-suppressor substrates. Systematic exploration of the structure-activity relationships of a previously known benzoxazinone compound led to the synthesis of A-893, a potent and selective SMYD2 inhibitor (IC50: 2.8 nM). A cocrystal structure reveals the origin of enhanced potency, and effective suppression of p53K370 methylation is observed in a lung carcinoma (A549) cell line.
PubMed: 26101576
DOI: 10.1021/acsmedchemlett.5b00124
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.79 Å)
構造検証レポート
Validation report summary of 4ynd
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2026-02-11に公開中

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