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BIOCHEMICAL JOURNAL (2008)
Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities
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Identification of novel protein kinase CK1 delta (CK1δ) inhibitors through structure-based virtual screening
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Identification of polyoxometalates as nanomolar noncompetitive inhibitors of protein kinase CK2
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Protein kinase CK2 in human diseases
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The catalytic subunit of human protein kinase CK2 structurally deviates from its maize homologue in complex with the nucleotide competitive inhibitor emodin
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The interaction of CK2α and CK2β, the subunits of protein kinase CK2, requires CK2β in a preformed conformation and is enthalpically driven
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The selectivity of protein kinase inhibitors: a further update
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BIOCHEMICAL JOURNAL (2007)
The ATP-binding site of protein kinase CK2 holds a positive electrostatic area and conserved water molecules
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Structure-based design, synthesis, and study of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase CK2
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BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2007)
Evolved to be active:: Sulfate ions define substrate recognition sites of CK2α and emphasise its exceptional role within the CMGC family of eukaryotic protein kinases
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Tetrabromocinnamic acid (TBCA) and related compounds represent a new class of specific protein kinase CK2 inhibitors
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Protein kinase CK2 inhibitor 4,5,6,7-tetrabromobenzotriazole (TBB) induces apoptosis and caspase-dependent degradation of haematopoietic lineage cell-specific protein 1 (HS1) in Jurkat cells
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