| Literature DB >> 30120148 |
Abstract
Defects in protein glycosylation can have a dramatic impact on eukaryotic cells and is associated with mental and developmental pathologies in humans. The studies outlined below illustrate how a basic biochemical problem in the mechanisms of protein glycosylation, specifically substrate transporters of nucleotide sugars, including ATP and 3'-phosphoadenyl-5'-phosphosulfate (PAPS), in the membrane of the Golgi apparatus and endoplasmic reticulum, expanded into diverse biological systems from mammals, including humans, to yeast, roundworms, and protozoa. Using these diverse model systems allowed my colleagues and me to answer fundamental biological questions that enabled us to formulate far-reaching hypotheses and expanded our knowledge of human diseases caused by malfunctions in the metabolic processes involved.Entities:
Keywords: Golgi; glycobiology; glycoprotein; glycoprotein biosynthesis; nucleotide
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Year: 2018 PMID: 30120148 PMCID: PMC6102126 DOI: 10.1074/jbc.X118.004819
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157