Phosphorylation-specific prolyl isomerization: is there an underlying theme?

Nat Cell Biol. 2005 May;7(5):435-41. doi: 10.1038/ncb0505-435.

Abstract

The prolyl isomerase Pin1 is a conserved enzyme that is intimately involved in diverse biological processes and pathological conditions such as cancer and Alzheimer's disease. By catalysing cis-trans interconversion of certain motifs containing phosphorylated serine or threonine residues followed by a proline residue (pSer/Thr-Pro), Pin1 can have profound effects on phosphorylation signalling. The structural and functional differences that result from cis-trans isomerization of specific pSer/Thr-Pro motifs probably underlie most, if not all, Pin1-dependent actions. Phosphorylation-dependent prolyl isomerization by Pin1 remains a unique mode for the modulation of signal transduction. Here, we provide an overview of the plethora of regulatory events that involve this unique enzyme, with a particular focus on oncogenic signalling and neurodegeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Cell Proliferation
  • Humans
  • Isomerism
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Peptidylprolyl Isomerase / chemistry
  • Peptidylprolyl Isomerase / metabolism*
  • Phosphorylation
  • Phosphoserine / metabolism
  • Phosphothreonine / metabolism
  • Protein Conformation
  • Signal Transduction / physiology*

Substances

  • NIMA-Interacting Peptidylprolyl Isomerase
  • Phosphothreonine
  • Phosphoserine
  • PIN1 protein, human
  • Peptidylprolyl Isomerase