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 |
---|---|---|---|---|
ST6GAL1 | CMP-Neu5Ac |
|
para-nitrophenol | |
ST8SIA6 | CMP-Neu5Ac |
|
||
ST6GALNAC2 | CMP-Neu5Ac |
|
para-nitrophenol | |
GAL3ST2 | PAPS |
|
[alpha]-benyzl | |
B4GALT2 | UDP-Gal |
|
Benzyl-[alpha] |
Pathway Name | Organism |
---|---|
E.coli O5ab | Escherichia coli |
E.coli O5ac | Escherichia coli |
E.coli O61 | Escherichia coli |
E.coli O65 | Escherichia coli |
E.coli O6H10K54 | Escherichia coli |
E.coli O6H16K15 | Escherichia coli |
E.coli O70 | Escherichia coli |
E.coli O71 | Escherichia coli |
E.coli O73ab | Escherichia coli |
E.coli O86 | Escherichia coli |
RES 1b:a-dgal-HEX-1:5 2s:n-acetyl LIN 1:1d(2+1)2n
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21799473 | Substrate Promiscuity of N-Acetylhexosamine 1-Kinases | Li Y | 2011 Jul 28 |
|
21999536 | Structural diversity of the core oligosaccharide domain of Pseudomonas aeruginosa lipopolysaccharide | Kocincova D | 2011 Jul |
|
21440051 | Bacterial adherence in otitis media: Determination of N-acetylgalactosamine (GalNAc) residues in the submucosal glands and surface epithelium of the normal and diseased Eustachian tube | Kirkeby S | 2011 Jul |
|
20473945 | Tumour‐associated glycan modifications of antigen enhance MGL2 dependent uptake and MHC class I restricted CD8 T cell responses | Singh SK | 2011 Jan 28 |
|
20934911 | A simple fibril and lectin model for cyst walls of Entamoeba and perhaps Giardia | Samuelson J | 2011 Jan |
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21307569 | Bacillus thuringiensisCry Toxins Bound Specifically to Various ProteinsviaDomain III, Which Had a Galactose-Binding Domain-Like Fold | KITAMI M | 2011 Feb 23 |
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21358053 | Modification of the sugar specificity of a plant lectin: structural studies on a point mutant ofErythrina corallodendronlectin | Thamotharan S | 2011 Feb 12 |
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21138417 | Chondroitin 4-O-sulfotransferase-1 regulates the chain length of chondroitin sulfate in co-operation with chondroitin N-acetylgalactosaminyltransferase-2 | Izumikawa T | 2011 Feb 11 |
|
21303815 | Structure of a lectin with antitumoral properties in king bolete (Boletus edulis) mushrooms | Bovi M | 2011 Feb 08 |
|
21300897 | Metabolic cross-talk allows labeling of O-linked beta-N-acetylglucosamine-modified proteins via the N-acetylgalactosamine salvage pathway | Boyce M | 2011 Feb 07 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 7, 2025