Organisms | Evidence |
---|---|
Ovis aries (sheep) | |
Cricetulus griseus (Chinese hamster) | |
Mus musculus (house mouse) | |
Bos taurus (domestic cattle) | |
Escherichia coli |
Gene Symbol | Donor | Acceptor | Reducing terminal(Acceptor) | Product | Reducing terminal(Product) | Reference |
---|---|---|---|---|---|---|
C1GALT1 | (not applicable) |
|
Ser/Thr |
|
Ser/Thr | |
ST6GALNAC1 | CMP-Neu5Ac |
|
Ser/Thr |
|
Ser/Thr | |
ST6GALNAC1 | CMP-Neu5Ac |
|
O-glycan Synthesis |
|
O-glycan Synthesis | |
B3GNT6 | UDP-GlcNAc |
|
[alpha]-pNP |
|
[alpha]-pNP |
Gene Symbol | Donor | Acceptor | Reducing terminal(Acceptor) | Product | Reducing terminal(Product) | Reference |
---|---|---|---|---|---|---|
C1GALT1 | (not applicable) |
|
Ser/Thr |
|
Ser/Thr | |
ST6GALNAC1 | CMP-Neu5Ac |
|
Ser/Thr |
|
Ser/Thr | |
ST6GALNAC4 | CMP-Neu5Ac |
|
benzyl |
|
benzyl | |
ST6GALNAC1 | CMP-Neu5Ac |
|
O-glycan Synthesis |
|
O-glycan Synthesis | |
ST6GALNAC1 | CMP-Neu5Ac |
|
[Ala-Thr(*)-Ala]2-7 |
|
[Ala-Thr(*)-Ala]2-7 |
Gene Symbol | Donor | Acceptor | Reducing terminal(Acceptor) | Reference |
---|---|---|---|---|
ST6GALNAC3 | CMP-Neu5Ac |
|
Ser/Thr | |
ST6GAL2 | CMP-Neu5Ac |
|
para-nitrophenol | |
ST6GALNAC2 | CMP-Neu5Ac |
|
benzyl | |
ST6GALNAC1 | CMP-Neu5Ac |
|
[alpha]-Bz | |
ST6GALNAC2 | CMP-Neu5Ac |
|
Ser/Thr |
Pathway Name | Organism |
---|---|
E.coli O128ac | Escherichia coli |
E.coli O138 | Escherichia coli |
E.coli O142 | Escherichia coli |
E.coli O154 | Escherichia coli |
E.coli O157 | Escherichia coli |
E.coli O158ab | Escherichia coli |
E.coli O166 | Escherichia coli |
E.coli O176 | Escherichia coli |
E.coli O184 | Escherichia coli |
E.coli O185 | Escherichia coli |
RES 1b:a-dgal-HEX-1:5 2s:n-acetyl LIN 1:1d(2+1)2n
PubMed ID | Title | First Author | Publication Date | Source |
---|---|---|---|---|
6254979 | Purification and properties of alpha-N-acetylgalactosaminidase from Clostridium perfringens. | Levy GN | 1980 Dec 25 |
|
6938955 | Oligosaccharide moieties of glycoprotein hormones: bovine lutropin resists enzymatic deglycosylation because of terminal O-sulfated N-acetylhexosamines. | Parsons TF | 1980 Dec |
|
6773807 | Evidence against the participation of lipid intermediates in the in vitro biosynthesis of serine(threonine)‐N‐acetyl‐D‐galactosamine linkages in submaxillary mucin | Babczinski P | 1980 Aug 11 |
|
7414948 | Adsorption and endo-glycosidase activity of phage phi 1 (40) on Salmonella johannesbureg O-polysaccharide | Chaby R | 1980 Aug |
|
7422356 | Characterization of the exposed carbohydrates on the surface membrane of adultSchistosoma mansoniby analysis of lectin binding | Simpson AJ | 1980 Aug |
|
6156677 | The relationship between the N-acetylgalactosamine content and the blood group Sda activity of Tamm and Horsfall urinary glycoprotein | Soh CPC | 1980 Apr 29 |
|
7378878 | Studies on the in vivo uptake and incorporation of 1-14C-labeled <scp>D</scp>-hexosamines in tissues, mucopolysaccharide–peptide complexes, and glycosaminoglycans of the domestic fowl | Kwai Hang KFN | 1980 Apr 01 |
|
7363947 | Concanavalin A affects polysaccharidic wall formation and mitotic activity in Polyphysa (Acetabularia) cliftonii protoplasts | Zimmer B | 1980 Apr |
|
7358487 | Effect of lectins on migration of the corneal epithelium | Gipson IK | 1980 Apr |
|
7192199 | Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22 | Geurts van Kessel AH | 1980 |
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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