Structure and function of phosphatidylinositol 3-kinase: a potential second messenger system involved in growth control

Philos Trans R Soc Lond B Biol Sci. 1993 Jun 29;340(1293):337-44. doi: 10.1098/rstb.1993.0076.

Abstract

Ligand stimulation of growth factor receptors with intrinsic protein-tyrosine kinase activity initiates the assembly of multienzyme signalling complexes. This is mediated by binding of proteins with src homology 2 (SH2) domains to receptor autophosphorylation sites. Among the proteins involved in complex formation is phosphatidylinositol (PI) 3-kinase, a heterodimeric enzyme composed of 85 kDa and 110 kDa subunits, which binds to receptor (and non-receptor) phosphotyrosine residues through the two SH2 domains in the p85 subunit. p85 acts as an adaptor protein and possibly a regulator of the p110 catalytic subunit that phosphorylates phosphoinositides at the D-3 position of the inositol ring. p85 subunit is composed of several distinct functional domains: one SH3 and two SH2 domains, a p110 binding site and a region with homology to BCR. Expression of these domains in E. coli as GST-fusion proteins has allowed definition by nuclear magnetic resonance (NMR) of three-dimensional structures for the SH2 and SH3 domains. The relationship of structure to function for these domains is discussed. The p110 catalytic domain has a region of homology with vps34p of Saccharomyces cerevisiae, a protein involved in protein sorting to the yeast vacuole. Possible clues to the function of PI 3-kinase derived from this and other observations are presented.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain / enzymology
  • Cattle
  • Gene Expression
  • Growth / physiology
  • Macromolecular Substances
  • Models, Biological
  • Molecular Sequence Data
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases / biosynthesis
  • Phosphotransferases / genetics
  • Phosphotransferases / metabolism*
  • Receptors, Cell Surface / metabolism
  • Second Messenger Systems*
  • Sequence Homology, Amino Acid

Substances

  • Macromolecular Substances
  • Receptors, Cell Surface
  • Phosphotransferases
  • Phosphatidylinositol 3-Kinases