articleJournal of Biological ChemistryApr 1, 2003HYBRID OA

Insulin-stimulated Phosphorylation of a Rab GTPase-activating Protein Regulates GLUT4 Translocation

Dartmouth College · Harvard University

PubMed
Indexed incrossrefdoajpubmed

Abstract

Insulin stimulates the rapid translocation of intracellular glucose transporters of the GLUT4 isotype to the plasma membrane in fat and muscle cells. The connections between known insulin signaling pathways and the protein machinery of this membrane-trafficking process have not been fully defined. Recently, we identified a 160-kDa protein in adipocytes, designated AS160, that is phosphorylated by the insulin-activated kinase Akt. This protein contains a GTPase-activating domain (GAP) for Rabs, which are small G proteins required for membrane trafficking. In the present study we have identified six sites of in vivo phosphorylation on AS160. These sites lie in the motif characteristic of Akt phosphorylation, and…

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Authors

8

Topics & keywords

Keywords
  • GLUT4
  • Rab
  • Protein kinase B
  • Phosphorylation
  • Cell biology
  • Glucose transporter
  • Biology
  • Insulin receptor
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