PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9878780-2	1999	alpha-Glucosidase I encoded by CWH41 cleaves the terminal alpha1, 2-linked glucose and alpha-glucosidase II encoded by ROT2 removes the two alpha1,3-linked glucose residues from the Glc3Man9GlcNAc2 oligosaccharide precursor while the alpha1,2-mannosidase encoded by MNS1 removes one specific mannose to form a single isomer of Man8GlcNAc2.	Oligosaccharides	198-213	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	31-36	
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	Oligosaccharides	122-138	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	270-275	
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	Oligosaccharides	122-138	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	399-404	
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	Oligosaccharides	237-253	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	270-275	
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	Oligosaccharides	237-253	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	399-404	
6381483-2	1984	Oligosaccharides on invertase, a secreted protein, and carboxypeptidase Y, a vacuolar protein, are matured normally in the gls1 mutant but retain three glucoses/carbohydrate chain.	Oligosaccharides	0-16	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	123-127	
6381483-3	1984	The gls1 mutation is recessive and extracts of mutant cells are inactive in release of labeled glucose from core oligosaccharides.	Oligosaccharides	113-129	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	4-8