Acyl transfer mechanisms of tissue transglutaminase

被引:73
作者
Keillor, Jeffrey W. [1 ]
Clouthier, Christopher M. [1 ]
Apperley, Kim Y. P. [1 ]
Akbar, Abdullah [1 ]
Mulani, Amina [1 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
关键词
Enzyme mechanism; Acyl transfer; Transglutaminase; Transamidation; PIG LIVER TRANSGLUTAMINASE; DISPLAYED PEPTIDE LIBRARY; CATALYZED CROSS-LINKING; AMINE-DONOR LYSINE; CONFORMATIONAL-CHANGES; STRUCTURAL BASIS; BINDING SITE; IDENTIFICATION; ENZYME; SPECIFICITY;
D O I
10.1016/j.bioorg.2014.06.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:186 / 197
页数:12
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