3FZ1

Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)

3FZ1 の概要

• エントリーDOI: 10.2210/pdb3fz1/pdb
• 関連するPDBエントリー: 1AQ1 3FYK
• 分子名称: Cell division protein kinase 2, (3R)-3-(aminomethyl)-9-methoxy-1,2,3,4-tetrahydro-5H-[1]benzothieno[3,2-e][1,4]diazepin-5-one (3 entities in total)
• 機能のキーワード: cdk-2, mk-2, mk2, mapkap kinase-2, ser/thr kinase, cell divison kinase-2, cyclin, benzothiophene, atp-binding, cell cycle, cell division, kinase, mitosis, nucleotide-binding, phosphoprotein, polymorphism, serine/threonine-protein kinase, transferase
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cytoplasm, cytoskeleton, microtubule organizing center, centrosome: P24941
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34253.83

構造登録者

Kurumbail, R.G.,Caspers, N. (登録日: 2009-01-23, 公開日: 2009-04-07, 最終更新日: 2023-09-06)

• 主引用文献: Anderson, D.R.,Meyers, M.J.,Kurumbail, R.G.,Caspers, N.,Poda, G.I.,Long, S.A.,Pierce, B.S.,Mahoney, M.W.,Mourey, R.J.,Parikh, M.D.; Benzothiophene inhibitors of MK2. Part 2: improvements in kinase selectivity and cell potency.; Bioorg.Med.Chem.Lett., 19:4882-4884, 2009; PubMed: 19616942; DOI: 10.1016/j.bmcl.2009.02.017

実験手法

X-RAY DIFFRACTION (1.9 Å)