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3ORX

PDK1 mutant bound to allosteric disulfide fragment inhibitor 1F8

Summary for 3ORX
Entry DOI10.2210/pdb3orx/pdb
Descriptor3-phosphoinositide-dependent protein kinase 1, 2-methyl-N-(2-sulfanylethyl)-1-benzofuran-3-carboxamide, CHLORIDE ION, ... (4 entities in total)
Functional Keywordspif pocket, c-helix, activation loop, agc kinase, transferase, allosteric inhibitor, phosphorylation, allostery, disulfide, kinase, pdk1, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: O15530
Total number of polymer chains8
Total formula weight291443.88
Authors
Sadowsky, J.D.,Wells, J.A. (deposition date: 2010-09-08, release date: 2011-03-23, Last modification date: 2023-09-06)
Primary citationSadowsky, 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: 21430264
DOI: 10.1073/pnas.1102376108
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2044 Å)
Structure validation

218500

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