Analysis of congenital disorder of glycosylation-id in a yeast model system shows diverse site-specific under-glycosylation of glycoproteins

Journal of Proteome Research

Volumn 11, Issue 11, 2012, Pages 5376-5383

  Bailey, Ulla Maja ^a   Jamaluddin, Muhammad Fairuz ^a   Schulz, Benjamin L ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

ALG; alg3; CDG; glycosylation occupancy; mass spectrometry; N glycosylation; oligosaccharyltransferase; PNGase F

Indexed keywords

ASPARAGINE; ASPARTIC ACID; GLYCOSIDASE;

ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1D; ELECTROSPRAY MASS SPECTROMETRY; GLYCOSYLATION; LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; PROTEIN CLEAVAGE; TANDEM MASS SPECTROMETRY; WILD TYPE;

AMINO ACID SEQUENCE; CELL WALL; CONGENITAL DISORDERS OF GLYCOSYLATION; GLYCOPROTEINS; GLYCOSYLATION; MODELS, BIOLOGICAL; MOLECULAR SEQUENCE DATA; PEPTIDE-N4-(N-ACETYL-BETA-GLUCOSAMINYL) ASPARAGINE AMIDASE; PROTEOLYSIS; SACCHAROMYCES CEREVISIAE; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; TRYPSIN;

EUKARYOTA; SACCHAROMYCES;

EID: 84868322234     PISSN: 15353893     EISSN: 15353907     Source Type: Journal    
DOI: 10.1021/pr300599f     Document Type: Article

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