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1 nd the beta subunit of endoplasmic reticulum glucosidase II.
2 ts to be the functional catalytic subunit of glucosidase II.
3 by the action of endomannosidase rather than glucosidase II.
4 protein tyrosine phosphatase 1B (PTP1B), and glucosidase II.
8 Ac2 as a substrate, it was demonstrated that glucosidase II activity was markedly down-regulated in m
9 chizosaccharomices pombe drastically reduces glucosidase II activity, but the role of the beta subuni
12 on, levels of normal hepatocystin and of the glucosidase II alpha subunit are substantially reduced i
15 structures of the main ERQC enzyme, ER alpha-glucosidase II (alpha-GluII; from mouse), alone and in c
16 unctions as the noncatalytic beta subunit of Glucosidase II, an endoplasmic reticulum (ER)-resident e
17 ions in PRKCSH, encoding the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in
18 nd yeast strains defective in glucosidase I, glucosidase II and BiP/Kar2p, it was demonstrated that c
19 ng and release are regulated by two enzymes, glucosidase II and UDP-Glc:glycoprotein:glycosyltransfer
20 (Ustilago maydis), glucosidase I (Gls1) and glucosidase II beta-subunit (Gas2), are essential for it
22 ponse to the posttranslational inhibition of glucosidase II, demonstrating that the attenuated remova
24 and genetic approaches, we demonstrate that glucosidase II (GII) mediates glycan trimming of TRPP2.
27 sylation of N-glycans, and oppositely acting glucosidase II (GlucII), and that vIL-6 can promote prot
29 similar to the glycoprotein-processing alpha-glucosidase II of mammalian and yeast origin than to oth
31 ycosidase F or removal of the glucoses by ER glucosidase II resulted in dissociation of the complexes
33 rate 80K-H" or "noncatalytic beta-subunit of glucosidase II." This protein is highly conserved, is ex
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