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Protein O-mannosylation: Conserved from bacteria to humans

期刊

GLYCOBIOLOGY
卷 19, 期 8, 页码 816-828

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/glycob/cwp066

关键词

congenital muscular dystrophy; glycosylation; mannosyltransferase; O-mannosylation

资金

  1. Deutsche Forschungsgemeinschaft
  2. European Union

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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.

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