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1 ted protein by the integral membrane protein oligosaccharyltransferase.
2 nsights on the function and the evolution of oligosaccharyltransferases.
3 sed to the signal peptide from accessing the oligosaccharyltransferase active site until the signal p
4 x. volcanii and deletion mutants lacking the oligosaccharyltransferase AglB suggests that when the Ag
5 ogs suggest that the enzymatic properties of oligosaccharyltransferase are regulated in eukaryotes to
7 saccharides added to a protein by the enzyme oligosaccharyltransferase can influence its expression a
8 kingly similar specificity as the classical, oligosaccharyltransferase-catalyzed N-glycosylation, wit
10 % identity to OST-48, a 48-kDa member of the oligosaccharyltransferase complex found in microsomal me
11 ediated by STT3a, a catalytic subunit of the oligosaccharyltransferase complex involved in co-transla
12 3, which encodes an essential subunit of the oligosaccharyltransferase complex that is involved in pr
13 n DDOST, whose product is a component of the oligosaccharyltransferase complex that transfers the gly
14 eostasis, an additional subunit of the human oligosaccharyltransferase complex, and a phosphatidylino
15 AGE-ligand and Western analyses of purified oligosaccharyltransferase complex, enriched rough endopl
16 ce that the TRAP complex, which binds to the oligosaccharyltransferase complex, is directly involved
19 to an accessory or regulatory subunit of the oligosaccharyltransferase enzyme complex in Saccharomyce
22 accharide is transferred by a membrane-bound oligosaccharyltransferase from a lipid donor to asparagi
24 dinated purified enzyme shows that the yeast oligosaccharyltransferase is composed of equimolar amoun
25 metazoan organisms, the STT3A isoform of the oligosaccharyltransferase is localized adjacent to the p
32 immune activation by interacting with the ER oligosaccharyltransferase (OST) complex and stabilizing
39 compared donor substrate utilization by the oligosaccharyltransferase (OST) from Trypanosoma cruzi,
40 ypanosomiasis and contains three full-length oligosaccharyltransferase (OST) genes; two of which, TbS
41 of Ribophorin 1, an integral protein of the oligosaccharyltransferase (OST) glycosylation complex.
42 nascent polypeptide chain is catalyzed by an oligosaccharyltransferase (OST) in the lumen of the endo
48 azoan organisms assemble two isoforms of the oligosaccharyltransferase (OST) that have different cata
49 inked glycoproteins, catalyzed by the enzyme oligosaccharyltransferase (OST), involves the transfer o
50 paragine-linked glycosylation pathway is the oligosaccharyltransferase (OST), PglB, which transfers p
51 ligosaccharides (LLOs) are the substrates of oligosaccharyltransferase (OST), the enzyme that catalyz
59 ning only 36 amino acids and is a subunit of oligosaccharyltransferase (OT) in Saccharomyces cerevisi
63 nadate-resistant mutant that is defective in oligosaccharyltransferase (OTase) activity both in vivo
64 ycosyltransferase, glycosyltransferases, and oligosaccharyltransferase (OTase) were analyzed in vitro
69 evious studies have shown that the bacterial oligosaccharyltransferase, PglB, of Campylobacter jejuni
70 homologue of ribophorin I, a subunit of the oligosaccharyltransferase-protein complex located in the
71 o patient sera, whereas deletion of the pglB oligosaccharyltransferase significantly reduced reactivi
74 subunit composition and stoichiometry of the oligosaccharyltransferase were investigated by attaching
75 o endogenous peptide acceptors via the yeast oligosaccharyltransferase when sealed vesicles were incu
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