4DEI

Crystal structure of c-Met in complex with triazolopyridinone inhibitor 24

4DEI の概要

• エントリーDOI: 10.2210/pdb4dei/pdb
• 関連するPDBエントリー: 4DEG 4DEh
• 分子名称: Hepatocyte growth factor receptor, 3-{(1S)-1-[3-(2-methoxyethoxy)quinolin-6-yl]ethyl}-5-(3-methyl-1,2-thiazol-5-yl)-3,5-dihydro-4H-[1,2,3]triazolo[4,5-c]pyridin-4-one (3 entities in total)
• 機能のキーワード: proto-oncogene, inhibitor, receptor tyrosine kinase, rtk, atp-binding, hepatocyte growth factor/scatter factor, hgf/sf, phosphoprotein, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Membrane; Single-pass type I membrane protein. Isoform 3: Secreted: P08581
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 35678.24

構造登録者

Whittington, D.A.,Long, A.M. (登録日: 2012-01-20, 公開日: 2012-05-30, 最終更新日: 2024-02-28)

• 主引用文献: Bode, C.M.,Boezio, A.A.,Albrecht, B.K.,Bellon, S.F.,Berry, L.,Broome, M.A.,Choquette, D.,Dussault, I.,Lewis, R.T.,Lin, M.H.,Rex, K.,Whittington, D.A.,Yang, Y.,Harmange, J.C.; Discovery and optimization of a potent and selective triazolopyridinone series of c-Met inhibitors.; Bioorg.Med.Chem.Lett., 22:4089-4093, 2012; PubMed: 22595176; DOI: 10.1016/j.bmcl.2012.04.072

実験手法

X-RAY DIFFRACTION (2.05 Å)