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3jy0
From Proteopedia
Discovery of 3H-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as Potent, Highly Selective and Orally Bioavailable Pim Kinases Inhibitors
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Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Stoll, V S | Alternative initiation | Atp-binding | Cell membrane | Kinase | Manganese | Membrane | Metal-binding | Nucleotide-binding | Nucleus | Phosphoprotein | Pim-1 | Proto-oncogene | Serine/threonine-protein kinase | Transferase
