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1 ted protein by the integral membrane protein oligosaccharyltransferase.
2 nsights on the function and the evolution of oligosaccharyltransferases.
3 sights into the addition of N-glycans by the oligosaccharyltransferases A and B (OST-A and OST-B).
4 sed to the signal peptide from accessing the oligosaccharyltransferase active site until the signal p
5 x. volcanii and deletion mutants lacking the oligosaccharyltransferase AglB suggests that when the Ag
6 e apply our methods to enrich membrane-bound oligosaccharyltransferases and lipid-linked oligosacchar
7 ated multi-omics profiling identified STT3A (oligosaccharyltransferase) and ALG5 (dolichyl-phosphate
8 ogs suggest that the enzymatic properties of oligosaccharyltransferase are regulated in eukaryotes to
10 saccharides added to a protein by the enzyme oligosaccharyltransferase can influence its expression a
11 kingly similar specificity as the classical, oligosaccharyltransferase-catalyzed N-glycosylation, wit
14 ion in humans is mediated exclusively by the oligosaccharyltransferase complex and is frequently hija
15 cted and validated STT3A/B proteins of the N-oligosaccharyltransferase complex as host targets of bro
16 , endoplasmic reticulum membrane complex and oligosaccharyltransferase complex components), along wit
17 % identity to OST-48, a 48-kDa member of the oligosaccharyltransferase complex found in microsomal me
18 While the structure of the eight-protein oligosaccharyltransferase complex has been determined re
19 r progression-associated upregulation of the oligosaccharyltransferase complex in epithelial cells.
20 ediated by STT3a, a catalytic subunit of the oligosaccharyltransferase complex involved in co-transla
21 or 4 (TLR4) is specifically dependent on the oligosaccharyltransferase complex OST-A for N-glycosylat
22 3, which encodes an essential subunit of the oligosaccharyltransferase complex that is involved in pr
23 n DDOST, whose product is a component of the oligosaccharyltransferase complex that transfers the gly
24 eostasis, an additional subunit of the human oligosaccharyltransferase complex, and a phosphatidylino
25 AGE-ligand and Western analyses of purified oligosaccharyltransferase complex, enriched rough endopl
26 ce that the TRAP complex, which binds to the oligosaccharyltransferase complex, is directly involved
33 ructural fold with the catalytic subunits of oligosaccharyltransferases, confirming a previously prop
34 to an accessory or regulatory subunit of the oligosaccharyltransferase enzyme complex in Saccharomyce
37 accharide is transferred by a membrane-bound oligosaccharyltransferase from a lipid donor to asparagi
39 so show that Manbeta1-4GlcNAc is produced by oligosaccharyltransferase hydrolysis of lipid-linked oli
40 dinated purified enzyme shows that the yeast oligosaccharyltransferase is composed of equimolar amoun
41 metazoan organisms, the STT3A isoform of the oligosaccharyltransferase is localized adjacent to the p
50 T1 has been described to be a subunit of the oligosaccharyltransferase (OST) complex and more specifi
51 immune activation by interacting with the ER oligosaccharyltransferase (OST) complex and stabilizing
53 he catalytic subunit of the STT3A-containing oligosaccharyltransferase (OST) complex, essential for p
54 OST48 is a non-catalytic component of the oligosaccharyltransferase (OST) complex, which transfers
59 etory pathway proteins are N-glycosylated by oligosaccharyltransferase (OST) complexes as they enter
62 t limited success due in part to the lack of oligosaccharyltransferase (OST) enzymes that can install
63 compared donor substrate utilization by the oligosaccharyltransferase (OST) from Trypanosoma cruzi,
64 ypanosomiasis and contains three full-length oligosaccharyltransferase (OST) genes; two of which, TbS
65 of Ribophorin 1, an integral protein of the oligosaccharyltransferase (OST) glycosylation complex.
66 nascent polypeptide chain is catalyzed by an oligosaccharyltransferase (OST) in the lumen of the endo
72 azoan organisms assemble two isoforms of the oligosaccharyltransferase (OST) that have different cata
73 inked glycoproteins, catalyzed by the enzyme oligosaccharyltransferase (OST), involves the transfer o
74 paragine-linked glycosylation pathway is the oligosaccharyltransferase (OST), PglB, which transfers p
75 ligosaccharides (LLOs) are the substrates of oligosaccharyltransferase (OST), the enzyme that catalyz
84 o acceptor polypeptides using single-subunit oligosaccharyltransferases (OSTs) from the eukaryotic pa
85 we adapt our workflow to study and engineer oligosaccharyltransferases (OSTs) involved in protein gl
86 ning only 36 amino acids and is a subunit of oligosaccharyltransferase (OT) in Saccharomyces cerevisi
90 nadate-resistant mutant that is defective in oligosaccharyltransferase (OTase) activity both in vivo
91 ycosyltransferase, glycosyltransferases, and oligosaccharyltransferase (OTase) were analyzed in vitro
96 evious studies have shown that the bacterial oligosaccharyltransferase, PglB, of Campylobacter jejuni
98 homologue of ribophorin I, a subunit of the oligosaccharyltransferase-protein complex located in the
99 o patient sera, whereas deletion of the pglB oligosaccharyltransferase significantly reduced reactivi
101 d after RNAi-based silencing of TbSTT3A, the oligosaccharyltransferase that transfers paucimannose st
103 bioconjugation hinges upon the ability of an oligosaccharyltransferase to efficiently transfer a poly
106 subunit composition and stoichiometry of the oligosaccharyltransferase were investigated by attaching
107 o endogenous peptide acceptors via the yeast oligosaccharyltransferase when sealed vesicles were incu
108 haride protein conjugate vaccine produced by oligosaccharyltransferases, which catalyze the en bloc t