4KZC
Structure of PI3K gamma with Imidazopyridine inhibitors
Summary for 4KZC
Entry DOI | 10.2210/pdb4kzc/pdb |
Related | 4KZ0 |
Descriptor | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, N-{6-[6-amino-5-(trifluoromethyl)pyridin-3-yl]imidazo[1,2-a]pyridin-2-yl}acetamide, SULFATE ION (3 entities in total) |
Functional Keywords | lipid kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: P48736 |
Total number of polymer chains | 1 |
Total formula weight | 111187.51 |
Authors | Knapp, M.S.,Elling, E.A. (deposition date: 2013-05-29, release date: 2013-07-17, Last modification date: 2024-02-28) |
Primary citation | Pecchi, S.,Ni, Z.J.,Han, W.,Smith, A.,Lan, J.,Burger, M.,Merritt, H.,Wiesmann, M.,Chan, J.,Kaufman, S.,Knapp, M.S.,Janssen, J.,Huh, K.,Voliva, C.F. Structure guided optimization of a fragment hit to imidazopyridine inhibitors of PI3K. Bioorg.Med.Chem.Lett., 23:4652-4656, 2013 Cited by PubMed: 23820386DOI: 10.1016/j.bmcl.2013.06.010 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.25 Å) |
Structure validation
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