An ATP-site on-off switch that restricts phosphatase accessibility of Akt

Sci Signal. 2012 May 8;5(223):ra37. doi: 10.1126/scisignal.2002618.

Abstract

The protein serine-threonine kinase Akt undergoes a substantial conformational change upon activation, which is induced by the phosphorylation of two critical regulatory residues, threonine 308 and serine 473. Paradoxically, treating cells with adenosine 5'-triphosphate (ATP)-competitive inhibitors of Akt results in increased phosphorylation of both residues. We show that binding of ATP-competitive inhibitors stabilized a conformation in which both phosphorylated sites were inaccessible to phosphatases. ATP binding also produced this protection of the phosphorylated sites, whereas interaction with its hydrolysis product adenosine 5'-diphosphate (ADP) or allosteric Akt inhibitors resulted in increased accessibility of these phosphorylated residues. ATP-competitive inhibitors mimicked ATP by targeting active Akt. Forms of Akt activated by an oncogenic mutation or myristoylation were more potently inhibited by the ATP-competitive inhibitors than was wild-type Akt. These data support a new model of kinase regulation, wherein nucleotides modulate an on-off switch in Akt through conformational changes, which is disrupted by ATP-competitive inhibitors.

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / metabolism*
  • Allosteric Regulation
  • Binding Sites
  • Models, Molecular
  • Phosphoric Monoester Hydrolases / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism*

Substances

  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Proto-Oncogene Proteins c-akt
  • Phosphoric Monoester Hydrolases

Associated data

  • PDB/4EKK
  • PDB/4EKL