3ORX
PDK1 mutant bound to allosteric disulfide fragment inhibitor 1F8
Summary for 3ORX
Entry DOI | 10.2210/pdb3orx/pdb |
Descriptor | 3-phosphoinositide-dependent protein kinase 1, 2-methyl-N-(2-sulfanylethyl)-1-benzofuran-3-carboxamide, CHLORIDE ION, ... (4 entities in total) |
Functional Keywords | pif pocket, c-helix, activation loop, agc kinase, transferase, allosteric inhibitor, phosphorylation, allostery, disulfide, kinase, pdk1, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: O15530 |
Total number of polymer chains | 8 |
Total formula weight | 291443.88 |
Authors | Sadowsky, J.D.,Wells, J.A. (deposition date: 2010-09-08, release date: 2011-03-23, Last modification date: 2023-09-06) |
Primary citation | Sadowsky, J.D.,Burlingame, M.A.,Wolan, D.W.,McClendon, C.L.,Jacobson, M.P.,Wells, J.A. Turning a protein kinase on or off from a single allosteric site via disulfide trapping. Proc.Natl.Acad.Sci.USA, 108:6056-6061, 2011 Cited by PubMed: 21430264DOI: 10.1073/pnas.1102376108 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2044 Å) |
Structure validation
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