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4KCG

Human dCK C4S-S74E mutant in complex with UDP and the DI-39 inhibitor

Summary for 4KCG
Entry DOI10.2210/pdb4kcg/pdb
DescriptorDeoxycytidine kinase, N-{2-[5-(4-{[(4,6-diaminopyrimidin-2-yl)sulfanyl]methyl}-5-propyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]ethyl}methanesulfonamide, URIDINE-5'-DIPHOSPHATE, ... (4 entities in total)
Functional Keywordsphosphoryl transfer, phosphorylation, deoxycytidine, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationNucleus: P27707
Total number of polymer chains2
Total formula weight67260.94
Authors
Nomme, J.,Lavie, A. (deposition date: 2013-04-24, release date: 2014-03-12, Last modification date: 2023-09-20)
Primary citationNathanson, D.A.,Armijo, A.L.,Tom, M.,Li, Z.,Dimitrova, E.,Austin, W.R.,Nomme, J.,Campbell, D.O.,Ta, L.,Le, T.M.,Lee, J.T.,Darvish, R.,Gordin, A.,Wei, L.,Liao, H.I.,Wilks, M.,Martin, C.,Sadeghi, S.,Murphy, J.M.,Boulos, N.,Phelps, M.E.,Faull, K.F.,Herschman, H.R.,Jung, M.E.,Czernin, J.,Lavie, A.,Radu, C.G.
Co-targeting of convergent nucleotide biosynthetic pathways for leukemia eradication.
J.Exp.Med., 211:473-486, 2014
Cited by
PubMed: 24567448
DOI: 10.1084/jem.20131738
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.09 Å)
Structure validation

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