6XRM

Crystal structure of human PI3K-gamma in complex with Compound 4

6XRM の概要

• エントリーDOI: 10.2210/pdb6xrm/pdb
• 関連するPDBエントリー: 6XRL
• 分子名称: Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, 5-[2-amino-3-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidin-5-yl]-2-[(1S)-1-cyclopropylethyl]-7-(trifluoromethyl)-2,3-dihydro-1H-isoindol-1-one, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: phosphoinositide 3-kinase gamma, inhibitor, immunosuppression, cancer, proteros, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 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: 109419.47

構造登録者

Walker, N.P.,Jeffrey, J.L. (登録日: 2020-07-13, 公開日: 2020-09-16, 最終更新日: 2024-03-06)

• 主引用文献: Drew, S.L.,Thomas-Tran, R.,Beatty, J.W.,Fournier, J.,Lawson, K.V.,Miles, D.H.,Mata, G.,Sharif, E.U.,Yan, X.,Mailyan, A.K.,Ginn, E.,Chen, J.,Wong, K.,Soni, D.,Dhanota, P.,Chen, P.Y.,Shaqfeh, S.G.,Meleza, C.,Pham, A.T.,Chen, A.,Zhao, X.,Banuelos, J.,Jin, L.,Schindler, U.,Walters, M.J.,Young, S.W.,Walker, N.P.,Leleti, M.R.,Powers, J.P.,Jeffrey, J.L.; Discovery of Potent and Selective PI3K gamma Inhibitors.; J.Med.Chem., 63:11235-11257, 2020; PubMed: 32865410; DOI: 10.1021/acs.jmedchem.0c01203

実験手法

X-RAY DIFFRACTION (2.88 Å)