6CJE

Crystal Structure of Mnk2-D228G in complex with Inhibitor

6CJE の概要

• エントリーDOI: 10.2210/pdb6cje/pdb
• 関連するPDBエントリー: 6cj5
• 分子名称: MAP kinase-interacting serine/threonine-protein kinase 2, ZINC ION, 4-[(9H-purin-6-yl)amino]benzamide, ... (4 entities in total)
• 機能のキーワード: transferase-transferase inhibitor complex, mnk1 inhibitor, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (Human)
• 細胞内の位置: Isoform 2: Nucleus, PML body. Isoform 1: Cytoplasm: Q9HBH9
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 35924.12

構造登録者

Han, Q. (登録日: 2018-02-26, 公開日: 2018-05-09, 最終更新日: 2023-10-04)

• 主引用文献: Reich, S.H.,Sprengeler, P.A.,Chiang, G.G.,Appleman, J.R.,Chen, J.,Clarine, J.,Eam, B.,Ernst, J.T.,Han, Q.,Goel, V.K.,Han, E.Z.R.,Huang, V.,Hung, I.N.J.,Jemison, A.,Jessen, K.A.,Molter, J.,Murphy, D.,Neal, M.,Parker, G.S.,Shaghafi, M.,Sperry, S.,Staunton, J.,Stumpf, C.R.,Thompson, P.A.,Tran, C.,Webber, S.E.,Wegerski, C.J.,Zheng, H.,Webster, K.R.; Structure-based Design of Pyridone-Aminal eFT508 Targeting Dysregulated Translation by Selective Mitogen-activated Protein Kinase Interacting Kinases 1 and 2 (MNK1/2) Inhibition.; J. Med. Chem., 61:3516-3540, 2018; PubMed: 29526098; DOI: 10.1021/acs.jmedchem.7b01795

実験手法

X-RAY DIFFRACTION (3.36 Å)