Journal article
Mutations in Glycosyltransferases and Glycosidases: Implications for Associated Diseases
X Gu, AS Kovacs, Y Myung, DB Ascher
Biomolecules | MDPI | Published : 2024
DOI: 10.3390/biom14040497
Abstract
Glycosylation, a crucial and the most common post-translational modification, coordinates a multitude of biological functions through the attachment of glycans to proteins and lipids. This process, predominantly governed by glycosyltransferases (GTs) and glycoside hydrolases (GHs), decides not only biomolecular functionality but also protein stability and solubility. Mutations in these enzymes have been implicated in a spectrum of diseases, prompting critical research into the structural and functional consequences of such genetic variations. This study compiles an extensive dataset from ClinVar and UniProt, providing a nuanced analysis of 2603 variants within 343 GT and GH genes. We conduct..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
No Statement Available