Structural elements determining the transglycosylating activity of
glycoside hydrolase family 57 glycogen branching enzymes
Abstract
Glycoside hydrolase family 57 glycogen branching enzymes (GH57GBE)
catalyze the formation of an α-1,6 glycosidic bond between α-1,4 linked
glucooliogosaccharides. As an atypical family, a limited number of
GH57GBEs have been biochemically characterized so far. This study aimed
at acquiring a better understanding of the GH57GBE family by a
systematic sequence-based bioinformatics analysis of almost 2,500 gene
sequences and determining the branching activity of several native and
mutant GH57GBEs. A correlation was found between a very low or even no
branching activity with the absence of a flexible loop, a tyrosine at
the loop tip, and two β-sheets.