3E3B
Crystal structure of catalytic subunit of human protein kinase CK2alpha prime with a potent indazole-derivative inhibitor
Summary for 3E3B
Entry DOI | 10.2210/pdb3e3b/pdb |
Descriptor | Casein kinase II subunit alpha', [1-(6-{6-[(1-methylethyl)amino]-1H-indazol-1-yl}pyrazin-2-yl)-1H-pyrrol-3-yl]acetic acid (3 entities in total) |
Functional Keywords | casein kinase 2, ck2alpha prime, ck2alpha inhibitor, selective kinase inhibitor, atp-binding, kinase, nucleotide-binding, polymorphism, serine/threonine-protein kinase, transferase, wnt signaling pathway |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 40536.40 |
Authors | Kinoshita, T.,Nakaniwa, T.,Tada, T. (deposition date: 2008-08-07, release date: 2009-03-03, Last modification date: 2023-11-01) |
Primary citation | Nakaniwa, T.,Kinoshita, T.,Sekiguchi, Y.,Tada, T.,Nakanishi, I.,Kitaura, K.,Suzuki, Y.,Ohno, H.,Hirasawa, A.,Tsujimoto, G. Structure of human protein kinase CK2alpha2 with a potent indazole-derivative inhibitor Acta Crystallogr.,Sect.F, 65:75-79, 2009 Cited by PubMed: 19193990DOI: 10.1107/S1744309108043194 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.2 Å) |
Structure validation
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