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MMDB Description
18878Crystal Structure of Human Protein Kinase CK2 Holoenzyme
23986Crystal Structure of the Catalytic Subunit of Human Protein Kinase CK2
23653Crystal Structure of a C-terminal Deletion Mutant of Human Protein Kinase CK2 Catalytic Subunit
47243Crystal Structure of the Catalytic Subunit of Protein Kinase CK2 (C-terminal Deletion Mutant 1-335) in Complex With Two Sulfate Ions
66830Crystal Structure of Catalytic Subunit of Protein Kinase CK2
70217Crystal Structure of Human CK2 Alpha Complexed With Ellagic Acid
61889High Ph-value Crystal Structure of Emodin in Complex With the Catalytic Subunit of Protein Kinase CK2
62437LOW Ph-value Crystal Structure of Emodin in Complex With the Catalytic Subunit of Protein Kinase CK2
69963Crystal Structure of Catalytic Subunit of Human Protein Kinase Ck2alpha Prime With a Potent Indazole-derivative Inhibitor
69741Inactive Conformation of Human Protein Kinase CK2 Catalytic Subunit
72644Crystal Structure of the Catalytic Subunit of Human Protein Kinase CK2 With 5,6-dichloro-1-beta-d- Ribofuranosylbenzimidazole
81902Human CK2 Catalytic Domain in Complex With a Difurane Derivative Inhibitor (Cpa)
81903Human CK2 Catalytic Domain in Complex With a Difurane Derivative Inhibitor (Amr)
87332Human CK2 Catalytic Domain in Complex With Cx-4945
87334Human CK2 Catalytic Domain in Complex With Amppn
88068Structure of a Human Ck2alpha Prime, the Paralog Isoform of the Catalytic Subunit of Protein Kinase CK2 From Homo Sapiens
87370Human CK2 Catalytic Domain in Complex With a Pyridocarbazole Derivative Inhibitor
87371Human CK2 Catalytic Domain in Complex With a Benzopyridoindole Derivative Inhibitor
87372Human CK2 Catalytic Domain in Complex With a Benzopyridoindole Derivative Inhibitor
91265Structure of Human Ck2alpha in Complex With the Atp-competitive Inhibitor 3-(4,5,6,7-tetrabromo-1h-benzotriazol-1-yl)propan-1-ol