N-terminal entrance loop of yeast Yps1 and O-glycosylation of substrates are determinant factors controlling the shedding activity of this GPI-anchored endopeptidase Microbial biochemistry, physiology and metabolism

BMC Microbiology

Volumn 15, Issue 1, 2015, Pages

  Dubé, Alexandre K ^a   Bélanger, Marc ^a   Gagnon Arsenault, Isabelle ^a   Bourbonnais, Yves ^a  

^a UNIVERSITÉ LAVAL   (Canada)

Author keywords

Fungal; Quality control O glycosylation; Shedding post ER; Yapsin N entrance loop Zymogen activation GPI protein

Indexed keywords

CELL SURFACE PROTEIN; FUNGAL PROTEIN; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; MANNOSYLTRANSFERASE; PROTEIN PMT2; PROTEIN PMT4; PROTEINASE; SERINE; THREONINE; UNCLASSIFIED DRUG; YPS1 PROTEIN; ASPARTIC PROTEINASE; GLYCOSYLPHOSPHATIDYLINOSITOL; PROTEIN BINDING; SACCHAROMYCES CEREVISIAE PROTEIN; YPS1 PROTEIN, S CEREVISIAE;

AMINO TERMINAL SEQUENCE; ARTICLE; CANDIDA PARAPSILOSIS; CANDIDA TROPICALIS; ENDOPLASMIC RETICULUM ASSOCIATED DEGRADATION; ENZYME ACTIVE SITE; ENZYME SUBSTRATE; FUNGAL STRAIN; IMAGE PROCESSING; IMMUNOREACTIVITY; NONHUMAN; PLASMID; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN CLEAVAGE; PROTEIN DOMAIN; PROTEIN GLYCOSYLATION; PROTEIN PROCESSING; PROTEIN PURIFICATION; PROTEIN SYNTHESIS; SACCHAROMYCES CEREVISIAE; SEQUENCE ALIGNMENT; AMINO ACID SEQUENCE; ENZYMOLOGY; GLYCOSYLATION; METABOLISM; MOLECULAR GENETICS; MOLECULAR MODEL; PROTEIN CONFORMATION; PROTEIN DEGRADATION; PROTEIN TRANSPORT;

AMINO ACID SEQUENCE; ASPARTIC ACID ENDOPEPTIDASES; GLYCOSYLATION; GLYCOSYLPHOSPHATIDYLINOSITOLS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN TRANSPORT; PROTEOLYSIS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS;

EID: 85018120336     PISSN: None     EISSN: 14712180     Source Type: Journal    
DOI: 10.1186/s12866-015-0380-1     Document Type: Article

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