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O-glycosylated

Jentoft, N., 1990. Wliy are proteins O-glycosylated Trends in Biochemical Sciences 155 291-294. [Pg.237]

The diamonds in Fig. 1 represent the point of O-glycosylation by tetrasac-charide 1. Asn-26 indicates the point of N-glycosylation by the complex oligosaccharide 2. [Pg.173]

PGE was isolated as desribed in Material and Methods. SDS-PAGE electrophoresis of purified protein showed a single band migrating at approximately 60 kDa. This observation is not in the agreement with the calculated molecular weight of 35 584. However a similar effect has been observed previously in case of PGI and PGC. Apart of the N-glycosylation which plays role in all PGs (Fig. 3), O-glycosylation may also be present as indicated by the band size shift after a treatment of PGE with O.IM NaOH (data not shown). [Pg.828]

IV. Structural Analysis of Glycopeptides and Glycoproteins Containing O-Glycosyl Linkages... [Pg.21]

Now that the general considerations concerning the 13C-n.m.r.-spec-tral data for O-glycosylated model compounds have been discussed, attention may be focused on some specific cases. Table IV gives the 13C-n.m.r.-spectral data for L-serine that has been glycosylated with various carbohydrates, such as a- and / -d-G1c, a- and /9-D-Gal, a- and / -d-Xyl, a-D-Man, and a-D-GalNAc. As mentioned earlier, the specific resonance-assignments to amino acid carbon atoms were based on chemical... [Pg.25]

As mentioned in the Introduction, a variety of unusual carbohydrate -protein linkages is found in Nature. These may be placed in several categories (i) carbohydrates O-glycosylated to jff-hydroxy amino acids (ii) carbohydrates S-glycosylated to cysteine (Hi) carbohydrates N-gly-cosylated to the N-terminal amino group of the protein or (iv) in some... [Pg.44]


See other pages where O-glycosylated is mentioned: [Pg.286]    [Pg.312]    [Pg.557]    [Pg.1248]    [Pg.177]    [Pg.509]    [Pg.189]    [Pg.193]    [Pg.287]    [Pg.289]    [Pg.1]    [Pg.4]    [Pg.10]    [Pg.25]    [Pg.27]    [Pg.28]    [Pg.34]    [Pg.35]    [Pg.47]    [Pg.137]    [Pg.139]    [Pg.141]    [Pg.143]    [Pg.145]    [Pg.147]    [Pg.149]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.159]    [Pg.160]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.167]    [Pg.169]    [Pg.171]    [Pg.173]    [Pg.175]    [Pg.177]    [Pg.178]    [Pg.179]   
See also in sourсe #XX -- [ Pg.149 , Pg.156 ]




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C-Glycosyl compounds N,O-protection

Glycosyl poly-O-acyl

Mucins type O-glycosylation

O-Glycosyl amino acids

O-Glycosyl derivatives

O-Glycosyl derivatives base-catalyzed elimination

O-Glycosyl derivatives enzymic reactions

O-Glycosyl derivatives hydrolysis with acid

O-Glycosyl derivatives mass spectra

O-Glycosyl derivatives synthetic

O-Glycosyl linkage

O-Glycosyl linkage model compounds

O-Glycosyl trichloroacetimidates

O-Glycosylation

O-Protected 3-Methoxy-2-pyridyloxy Glycosyl Donors

Oligosaccharide Synthesis by Remote Activation O-Protected 3-Methoxy-2-pyridyloxy (MOP) Glycosyl Donors

Oligosaccharide Synthesis by Remote Activation O-Protected Glycosyl 2-thiopyridylcarbonate Donors

Phosphinates O-glycosylation

Phosphonates O-glycosylation

Structural Analysis of Glycopeptides and Glycoproteins Containing O-Glycosyl Linkages

Synthetic N- and O-glycosyl derivatives

Tether-Directed O-Glycosylation

The Twenty First Century View of Chemical O-Glycosylation

Threonine O-glycosyl derivatives

Threonine O-glycosylation

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