| Literature DB >> 25035302 |
Jeffrey W Keillor1, Christopher M Clouthier2, Kim Y P Apperley2, Abdullah Akbar2, Amina Mulani2.
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.Entities:
Keywords: Acyl transfer; Enzyme mechanism; Transamidation; Transglutaminase
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Year: 2014 PMID: 25035302 DOI: 10.1016/j.bioorg.2014.06.003
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275