TY - JOUR T1 - A phosphoproteomic approach reveals that PKD3 controls PKA-mediated glucose and tyrosine metabolism JF - Life Science Alliance JO - Life Sci. Alliance DO - 10.26508/lsa.202000863 VL - 4 IS - 8 SP - e202000863 AU - Angel Loza-Valdes AU - Alexander E Mayer AU - Toufic Kassouf AU - Jonathan Trujillo-Viera AU - Werner Schmitz AU - Filip Dziaczkowski AU - Michael Leitges AU - Andreas Schlosser AU - Grzegorz Sumara Y1 - 2021/08/01 UR - https://www.life-science-alliance.org/content/4/8/e202000863.abstract N2 - Members of the protein kinase D (PKD) family (PKD1, 2, and 3) integrate hormonal and nutritional inputs to regulate complex cellular metabolism. Despite the fact that a number of functions have been annotated to particular PKDs, their molecular targets are relatively poorly explored. PKD3 promotes insulin sensitivity and suppresses lipogenesis in the liver of animals fed a high-fat diet. However, its substrates are largely unknown. Here we applied proteomic approaches to determine PKD3 targets. We identified more than 300 putative targets of PKD3. Furthermore, biochemical analysis revealed that PKD3 regulates cAMP-dependent PKA activity, a master regulator of the hepatic response to glucagon and fasting. PKA regulates glucose, lipid, and amino acid metabolism in the liver, by targeting key enzymes in the respective processes. Among them the PKA targets phenylalanine hydroxylase (PAH) catalyzes the conversion of phenylalanine to tyrosine. Consistently, we showed that PKD3 is activated by glucagon and promotes glucose and tyrosine levels in hepatocytes. Therefore, our data indicate that PKD3 might play a role in the hepatic response to glucagon. ER -