7A22
Crystal structure of human protein kinase CK2alpha' (CSNK2A2 gene product) in complex with the ATP-competitive inhibitor 5,6,7-tribromo-1H-triazolo[4,5-b]pyridine
Summary for 7A22
Entry DOI | 10.2210/pdb7a22/pdb |
Related | 7A1B 7A1Z |
Descriptor | Casein kinase II subunit alpha', 1,2-ETHANEDIOL, 5,6,7-tris(bromanyl)-1~{H}-[1,2,3]triazolo[4,5-b]pyridine, ... (4 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 | 44043.55 |
Authors | Niefind, K.,Lindenblatt, D.,Toelzer, C.,Bretner, M.,Chojnacki, K.,Wielechowska, M.,Winska, P. (deposition date: 2020-08-15, release date: 2020-12-09, Last modification date: 2024-05-15) |
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 (1.01 Å) |
Structure validation
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