7A2H

Crystal structure of human protein kinase CK2alpha' (CSNK2A2 gene product) in complex with the ATP-competitive inhibitor 5,6,7-tribromo-1H-imidazo[4,5-b]pyridine

Summary for 7A2H

Entry DOI	10.2210/pdb7a2h/pdb
Related	7A1B 7A1Z 7A22
Descriptor	Casein kinase II subunit alpha', 5,6,7-tris(bromanyl)-1~{H}-imidazo[4,5-b]pyridine, 1,2-ETHANEDIOL, ... (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	43421.88
Authors	Niefind, K.,Lindenblatt, D.,Toelzer, C.,Bretner, M.,Chojnacki, K.,Wielechowska, M.,Winska, P. (deposition date: 2020-08-18, 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: 33317841 DOI: 10.1016/j.bioorg.2020.104502 PDB entries with the same primary citation
Experimental method	X-RAY DIFFRACTION (1.01 Å)

Structure validation