3UYT
crystal structure of ck1d with PF670462 from P1 crystal form
Summary for 3UYT
Entry DOI | 10.2210/pdb3uyt/pdb |
Related | 1CKI 3UYS 3UZP |
Descriptor | Casein kinase I isoform delta, 4-[1-cyclohexyl-4-(4-fluorophenyl)-1H-imidazol-5-yl]pyrimidin-2-amine, SULFATE ION, ... (4 entities in total) |
Functional Keywords | ck1d, kinase, inhibitor, pf670462, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: P48730 |
Total number of polymer chains | 4 |
Total formula weight | 139424.66 |
Authors | Huang, X. (deposition date: 2011-12-06, release date: 2012-01-11, Last modification date: 2024-02-28) |
Primary citation | Long, A.,Zhao, H.,Huang, X. Structural basis for the interaction between casein kinase 1 delta and a potent and selective inhibitor. J.Med.Chem., 55:956-960, 2012 Cited by PubMed Abstract: Casein kinase 1 delta (CK1δ) and its closest homologue CK1ε are key regulators of diverse cellular growth and survival processes such as Wnt signaling, DNA repair, and circadian rhythms. We report three crystal structures of the kinase domain of human CK1δ, one apo and two complexed with a potent and selective CK1δ/ε inhibitor PF670462 in two different crystal forms. These structures provide a molecular basis for the strong and specific inhibitor interactions and suggest clues for further development of CK1δ/ε inhibitors. PubMed: 22168824DOI: 10.1021/jm201387s PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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