3APF
Crystal structure of human PI3K-gamma in complex with CH5039699
Summary for 3APF
Entry DOI | 10.2210/pdb3apf/pdb |
Related | 3APC 3APD |
Descriptor | Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, SULFATE ION, 3-[7-(1H-benzimidazol-5-yl)-2-(morpholin-4-yl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]phenol, ... (4 entities in total) |
Functional Keywords | phosphoinositide 3-kinase gamma, kinase, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 111054.39 |
Authors | Nakamura, M.,Fukami, T.A.,Miyazaki, T.,Yoshida, M. (deposition date: 2010-10-14, release date: 2011-04-13, Last modification date: 2023-11-01) |
Primary citation | Ohwada, J.,Ebiike, H.,Kawada, H.,Tsukazaki, M.,Nakamura, M.,Miyazaki, T.,Morikami, K.,Yoshinari, K.,Yoshida, M.,Kondoh, O.,Kuramoto, S.,Ogawa, K.,Aoki, Y.,Shimma, N. Discovery and biological activity of a novel class I PI3K inhibitor, CH5132799 Bioorg.Med.Chem.Lett., 21:1767-1772, 2011 Cited by PubMed: 21316229DOI: 10.1016/j.bmcl.2011.01.065 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.82 Å) |
Structure validation
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