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3NAX

PDK1 in complex with inhibitor MP7

Summary for 3NAX
Entry DOI10.2210/pdb3nax/pdb
Related3NAY
Descriptor3-phosphoinositide-dependent protein kinase 1, 1-(3,4-difluorobenzyl)-2-oxo-N-{(1R)-2-[(2-oxo-2,3-dihydro-1H-benzimidazol-5-yl)oxy]-1-phenylethyl}-1,2-dihydropyridine-3-carboxamide (3 entities in total)
Functional Keywordskinase, serine/threonine protein kinase, transferase
Biological sourceHomo sapiens
Cellular locationCytoplasm: O15530
Total number of polymer chains1
Total formula weight36610.96
Authors
Yan, Y.,Munshi, S.K.,Allison, T. (deposition date: 2010-06-02, release date: 2010-11-24, Last modification date: 2024-02-21)
Primary citationNagashima, K.,Shumway, S.D.,Sathyanarayanan, S.,Chen, A.H.,Dolinski, B.,Xu, Y.,Keilhack, H.,Nguyen, T.,Wiznerowicz, M.,Li, L.,Lutterbach, B.A.,Chi, A.,Paweletz, C.,Allison, T.,Yan, Y.,Munshi, S.K.,Klippel, A.,Kraus, M.,Bobkova, E.V.,Deshmukh, S.,Xu, Z.,Mueller, U.,Szewczak, A.A.,Pan, B.S.,Richon, V.,Pollock, R.,Blume-Jensen, P.,Northrup, A.,Andersen, J.N.
Genetic and pharmacological inhibition of PDK1 in cancer cells: characterization of a selective allosteric kinase inhibitor.
J.Biol.Chem., 286:6433-6448, 2011
Cited by
PubMed: 21118801
DOI: 10.1074/jbc.M110.156463
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

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