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4KZC

Structure of PI3K gamma with Imidazopyridine inhibitors

Summary for 4KZC
Entry DOI10.2210/pdb4kzc/pdb
Related4KZ0
DescriptorPhosphatidylinositol 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 Keywordslipid kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P48736
Total number of polymer chains1
Total formula weight111187.51
Authors
Knapp, M.S.,Elling, E.A. (deposition date: 2013-05-29, release date: 2013-07-17, Last modification date: 2024-02-28)
Primary citationPecchi, 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: 23820386
DOI: 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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