Acyl transfer mechanisms of tissue transglutaminase

Bioorg Chem. 2014 Dec:57:186-197. doi: 10.1016/j.bioorg.2014.06.003. Epub 2014 Jun 25.

Abstract

Tissue transglutaminase (TG2) is a calcium-dependent enzyme that catalyses several acyl transfer reactions. The most biologically relevant of these involve protein-bound Gln residues as an acyl-donor substrate, and either water or a primary amine as an acyl-acceptor substrate. The former leads to deamidation of Gln to Glu, whereas the latter leads to transamidation, typically resulting in protein cross-linking when the amine substrate is a protein-bound Lys residue. In this review, we present an overview of over fifty years of mechanistic studies that have led to our current understanding of TG2-mediated hydrolysis and transamidation.

Keywords: Acyl transfer; Enzyme mechanism; Transamidation; Transglutaminase.

Publication types

  • Review

MeSH terms

  • Acylation
  • Animals
  • GTP-Binding Proteins / chemistry
  • GTP-Binding Proteins / metabolism*
  • Humans
  • Hydrolysis
  • Models, Molecular
  • Protein Conformation
  • Protein Glutamine gamma Glutamyltransferase 2
  • Substrate Specificity
  • Transglutaminases / chemistry
  • Transglutaminases / metabolism*

Substances

  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • GTP-Binding Proteins