6XRL
Crystal structure of human PI3K-gamma in complex with inhibitor IPI-549
6XRL の概要
エントリーDOI | 10.2210/pdb6xrl/pdb |
分子名称 | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, 2-amino-N-[(1S)-1-{8-[(1-methyl-1H-pyrazol-4-yl)ethynyl]-1-oxo-2-phenyl-1,2-dihydroisoquinolin-3-yl}ethyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide, 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 | 109466.57 |
構造登録者 | |
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 Cited by PubMed: 32865410DOI: 10.1021/acs.jmedchem.0c01203 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.99 Å) |
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