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4G16

Crystal structure of ck1g3 with 2-[(4-{[3-(TRIFLUOROMETHYL)PYRIDIN2-YL]OXY}PHENYL)AMINO]-1H-BENZIMIDAZOLE-6-CARBONITRILE

Summary for 4G16
Entry DOI10.2210/pdb4g16/pdb
Related4G17
DescriptorCasein kinase I isoform gamma-3, 2-[(4-{[3-(trifluoromethyl)pyridin-2-yl]oxy}phenyl)amino]-1H-benzimidazole-6-carbonitrile (3 entities in total)
Functional Keywordsck1g, kinase, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: Q9Y6M4
Total number of polymer chains1
Total formula weight38864.56
Authors
Huang, X. (deposition date: 2012-07-10, release date: 2013-05-22, Last modification date: 2023-09-13)
Primary citationHua, Z.,Huang, X.,Bregman, H.,Chakka, N.,DiMauro, E.F.,Doherty, E.M.,Goldstein, J.,Gunaydin, H.,Huang, H.,Mercede, S.,Newcomb, J.,Patel, V.F.,Turci, S.M.,Yan, J.,Wilson, C.,Martin, M.W.
2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1g)inhibitors
Bioorg.Med.Chem.Lett., 22:5392-5395, 2012
Cited by
PubMed: 22877629
DOI: 10.1016/j.bmcl.2012.07.046
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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