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7A5L

tructure of DYRK1A in complex with compound 24

7A5L の概要
エントリーDOI10.2210/pdb7a5l/pdb
関連するPDBエントリー7a4o 7a4r 7a4s 7a4w 7a4z 7a51 7a52 7a53 7a55 7a5b 7a5d
分子名称Dual specificity tyrosine-phosphorylation-regulated kinase 1A, 4-[2-methyl-4-(thiophen-3-ylmethoxy)-7~{H}-pyrrolo[2,3-d]pyrimidin-5-yl]pyridin-2-amine, CHLORIDE ION, ... (4 entities in total)
機能のキーワードserine/threonine-protein kinase, phosphoprotein, kinase, sbdd, fbld, small molecule inhibitor, transferase
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42019.98
構造登録者
Dokurno, P.,Surgenor, A.E.,Hubbard, R.E. (登録日: 2020-08-21, 公開日: 2021-06-30, 最終更新日: 2024-10-16)
主引用文献Lee Walmsley, D.,Murray, J.B.,Dokurno, P.,Massey, A.J.,Benwell, K.,Fiumana, A.,Foloppe, N.,Ray, S.,Smith, J.,Surgenor, A.E.,Edmonds, T.,Demarles, D.,Burbridge, M.,Cruzalegui, F.,Kotschy, A.,Hubbard, R.E.
Fragment-Derived Selective Inhibitors of Dual-Specificity Kinases DYRK1A and DYRK1B.
J.Med.Chem., 64:8971-8991, 2021
Cited by
PubMed Abstract: The serine/threonine kinase DYRK1A has been implicated in regulation of a variety of cellular processes associated with cancer progression, including cell cycle control, DNA damage repair, protection from apoptosis, cell differentiation, and metastasis. In addition, elevated-level DYRK1A activity has been associated with increased severity of symptoms in Down's syndrome. A selective inhibitor of DYRK1A could therefore be of therapeutic benefit. We have used fragment and structure-based discovery methods to identify a highly selective, well-tolerated, brain-penetrant DYRK1A inhibitor which showed in vivo activity in a tumor model. The inhibitor provides a useful tool compound for further exploration of the effect of DYRK1A inhibition in models of disease.
PubMed: 34143631
DOI: 10.1021/acs.jmedchem.1c00024
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.1 Å)
構造検証レポート
Validation report summary of 7a5l
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2025-02-05に公開中

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