3L54
Structure of Pi3K gamma with inhibitor
Summary for 3L54
Entry DOI | 10.2210/pdb3l54/pdb |
Related | 3L08 |
Descriptor | Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, SULFATE ION, 6-(1H-pyrazolo[3,4-b]pyridin-5-yl)-4-pyridin-4-ylquinoline, ... (4 entities in total) |
Functional Keywords | pi3k, pi3k gamma, phosphatidylinositol, pi3, atp-binding, kinase, nucleotide-binding, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: P48736 |
Total number of polymer chains | 1 |
Total formula weight | 111134.52 |
Authors | Elkins, P.A.,Smallwood, A.M. (deposition date: 2009-12-21, release date: 2010-06-30, Last modification date: 2024-02-21) |
Primary citation | Knight, S.D.,Adams, N.D.,Burgess, J.L.,Chaudhari, A.M.,Darcy, M.G.,Donatelli, C.A.,Luengo, J.I.,Newlander, K.A.,Parrish, C.A.,Ridgers, L.H.,Sarpong, M.A.,Schmidt, S.J.,Van Aller, G.S.,Carson, J.D.,Diamond, M.A.,Elkins, P.A.,Gardiner, C.M.,Garver, E.,Gilbert, S.A.,Gontarek, R.R.,Jackson, J.R.,Kershner, K.L.,Luo, L.,Raha, K.,Sherk, C.S.,Sung, C.M.,Sutton, D.,Tummino, P.J.,Wegrzyn, R.J.,Auger, K.R.,Dhanak, D. Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin. ACS Med Chem Lett, 1:39-43, 2010 Cited by PubMed: 24900173DOI: 10.1021/ml900028r PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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