PDK-1


PDH (Pyruvate dehydrogenase) is a part of a mitochondrial multienzyme complex that catalyzes the oxidative decarboxylation of pyruvate and is one of the major enzymes responsible for the regulation of homeostasis of carbohydrate fuels in mammals. The enzymatic activity is regulated by a phosphorylation/dephosphorylation cycle. Phosphorylation of PDH by a specific pyruvate dehydrogenase kinase (PDK) results in inactivation. In humans, there have been four isozymes of Pyruvate Dehydrogenase Kinase that have been shown to phosphorylate these three sites: PDK1, PDK2, PDK3, and PDK4. PDK1 is the only enzyme capable of phosphorylating the 3rd serine site. When the TPP coenzyme is bound, the rates of phosphorylation by all four isozymes are drastically affected; specifically, the incorporation of phosphate groups by PDK1 into sites 2 and 3 is significantly reduced
  • BX-912 EY0757

    BX-912是一种有效的,特异性的PDK1抑制剂,IC50为12 nM,作用于PKD1比作用于PKA和PKC选择性分别高9和105倍。

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  • PHT-427 EY0265

    PHT-427是作用于Akt和PDPK1的双重抑制剂,Akt和PDPK1的PH结构域具有高度亲和力,Ki分别为2.7 μM和5.2 μM。

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