5QU0

TGF-BETA RECEPTOR TYPE 1 KINASE DOMAIN (T204D) IN COMPLEX WITH 6-[4-(3-CHLORO-4-FLUOROPHENYL)-1-(2-HYDROXYETHYL)-1H-IMIDAZOL-5-YL]IMIDAZO[1,2-B]PYRIDAZINE-3-CARBONITRILE

5QU0 の概要

• エントリーDOI: 10.2210/pdb5qu0/pdb
• Group deposition: Crystal Structures of TGF-beta receptor type 1 kinase domain (T204D) (G_1002109)
• 分子名称: TGF-beta receptor type-1, 6-[4-(3-chloro-4-fluorophenyl)-1-(2-hydroxyethyl)-1H-imidazol-5-yl]imidazo[1,2-b]pyridazine-3-carbonitrile, GLYCEROL, ... (4 entities in total)
• 機能のキーワード: alk5, kinase domain, transferase-transferase inhibitor complex, 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: 35640.35

構造登録者

Sheriff, S. (登録日: 2019-11-19, 公開日: 2020-02-05, 最終更新日: 2024-05-22)

• 主引用文献: Velaparthi, U.,Darne, C.P.,Warrier, J.,Liu, P.,Rahaman, H.,Augustine-Rauch, K.,Parrish, K.,Yang, Z.,Swanson, J.,Brown, J.,Dhar, G.,Anandam, A.,Holenarsipur, V.K.,Palanisamy, K.,Wautlet, B.S.,Fereshteh, M.P.,Lippy, J.,Tebben, A.J.,Sheriff, S.,Ruzanov, M.,Yan, C.,Gupta, A.,Gupta, A.K.,Vetrichelvan, M.,Mathur, A.,Gelman, M.,Singh, R.,Kinsella, T.,Murtaza, A.,Fargnoli, J.,Vite, G.,Borzilleri, R.M.; Discovery of BMS-986260, a Potent, Selective, and Orally Bioavailable TGF beta R1 Inhibitor as an Immuno-oncology Agent.; Acs Med.Chem.Lett., 11:172-178, 2020; PubMed: 32071685; DOI: 10.1021/acsmedchemlett.9b00552

実験手法

X-RAY DIFFRACTION (1.67 Å)