7A1B
Crystal structure of human protein kinase CK2alpha' (CSNK2A2 gene product) in complex with the ATP-competitive inhibitor 5,6-dibromo-1H-triazolo[4,5-b]pyridine
Summary for 7A1B
Entry DOI | 10.2210/pdb7a1b/pdb |
Descriptor | Casein kinase II subunit alpha', 5,6-dibromo-1H-triazolo[4,5-b]pyridine, 1,2-ETHANEDIOL, ... (6 entities in total) |
Functional Keywords | protein kinase ck2, casein kinase 2, atp-competitive inhibitor, transferase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 43624.08 |
Authors | Niefind, K.,Lindenblatt, D.,Toelzer, C.,Bretner, M.,Chojnacki, K.,Wielechowska, M.,Winska, P. (deposition date: 2020-08-12, release date: 2020-12-09, Last modification date: 2021-01-13) |
Primary citation | Chojnacki, K.,Lindenblatt, D.,Winska, P.,Wielechowska, M.,Toelzer, C.,Niefind, K.,Bretner, M. Synthesis, biological properties and structural study of new halogenated azolo[4,5-b]pyridines as inhibitors of CK2 kinase. Bioorg.Chem., 106:104502-104502, 2021 Cited by PubMed: 33317841DOI: 10.1016/j.bioorg.2020.104502 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.287 Å) |
Structure validation
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