Protein O-mannosylation: conserved from bacteria to humans

Glycobiology. 2009 Aug;19(8):816-28. doi: 10.1093/glycob/cwp066. Epub 2009 May 9.

Abstract

Protein O-mannosylation is an essential modification in fungi and animals. Different from most other types of O-glycosylation, protein O-mannosylation is initiated in the endoplasmic reticulum by the transfer of mannose from dolichol monophosphate-activated mannose to serine and threonine residues of secretory proteins. In recent years, it has emerged that even bacteria are capable of O-mannosylation and that the biosynthetic pathway of O-mannosyl glycans is conserved between pro- and eukaryotes. In this review, we summarize the observations that have opened up the field and highlight characteristics of O-mannosylation in the different domains/kingdoms of life.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Bacterial Proteins / metabolism
  • Endoplasmic Reticulum / physiology*
  • Fungal Proteins / metabolism
  • Fungi / metabolism
  • Glycosylation
  • Humans
  • Mannose / metabolism*
  • Mannosyltransferases / metabolism*
  • Phylogeny
  • Polysaccharides / metabolism*
  • Protein Processing, Post-Translational / physiology*
  • Serine / metabolism
  • Threonine / metabolism

Substances

  • Bacterial Proteins
  • Fungal Proteins
  • Polysaccharides
  • Threonine
  • Serine
  • Mannosyltransferases
  • Mannose