glycosyltransferase secretion

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UNIPROT ID/AC

O45713 (7)
O45712 (7)
Q19813 (7)
Q86NE2 (7)
Q23150 (7)
Q09497 (7)
Q9N384 (7)
Q23258 (7)
P18833 (7)
O45105 (7)
K7ZUH9 (7)
P18835 (7)
WBGene00044737 (7)
WBGene00004424 (7)
WBGene00000293 (7)
Q9XXU9 (7)
Q9XXK1 (7)
Q9XX57 (7)
Q9XWT3 (7)
Q9XW92 (7)
Q9XVP0 (7)
Q9XVM0 (7)
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Q9UB28 (7)
Q9UAV5 (7)

CHEBI ID

CHEBI:17754 (2)
CHEBI:30915 (2)
CHEBI:17268 (2)
CHEBI:15428 (2)
CHEBI:193564 (1)
CHEBI:193563 (1)
CHEBI:182172 (1)
CHEBI:177932 (1)
CHEBI:47006 (1)
CHEBI:150213 (1)
CHEBI:28409 (1)
CHEBI:143542 (1)
CHEBI:150326 (1)
CHEBI:52417 (1)
CHEBI:192804 (1)
CHEBI:143036 (1)
CHEBI:177944 (1)
CHEBI:27347 (1)
CHEBI:187907 (1)
CHEBI:25899 (1)
CHEBI:79285 (1)
CHEBI:140436 (1)
CHEBI:15440 (1)
CHEBI:16971 (1)
CHEBI:55481 (1)
CHEBI:26849 (1)
CHEBI:18384 (1)
CHEBI:29042 (1)
CHEBI:33828 (1)
CHEBI:17733 (1)

Metabolite Name

L-Aspartate (2)
Ferulic acid (2)
Ursodeoxycholic acid (2)
Glycerol (2)
Lithocholic acid (2)
L-Arginine (2)
L-Alanine (2)
L-Threonine (2)
Creatinine (2)
L-Tyrosine (2)
Creatine (2)
2-(1-methyl-2-pyrrolidinyl)-pyridine (1)
2-ketoglucose dimethylacetal (1)
Conduritol-beta-expoxide (1)
Erythronic acid lactone (1)
Fructose-1-phosphate (1)
Isochlorogenic acid (1)
Isogluconic acid (1)
Isoribose (1)
Mannonic acid (1)
Saccharic acid (1)
Tocopherol alpha- (1)
Tocopherol beta (1)
Tocopherol delta- (1)
Tocopherol gamma- (1)
Triacontanol (1)
UDP-Galactose (Manual) (1)
Xylonolactone (1)
Isopropylbenzene (1)
Maleimide (1)

Study type

Transcription profiling by array (6)
RNA-seq of coding RNA from single cells (3)
RNA-seq of coding RNA (3)
Unknown experiment type (2)
Genotyping by array (1)
DNA-seq (1)

Release Date

2025 (9)
2020 (8)
2010 (5)
2022 (5)
2024 (4)
2023 (4)
2021 (4)
2019 (4)
2017 (4)
2026 (3)
2018 (3)
2016 (3)
2013 (3)
2011 (3)
2008 (3)
2015 (3)
2009 (2)
2003 (1)
2014 (1)
2012 (1)
2006 (1)

Lab affiliation

Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, Victoria, Australia (1)
NIDCR, NIH (1)
Institute of biochemistry and molecular biology, Bonn (1)
Centre for Innate Immunity and Infectious Diseases, HudsonInstitute of Medical Research, Clayton, Victoria, Australia (1)
College of Veterinary Medicine, Kansas State University, Manhattan, KS, United States (1)
Department of Microbiology and Immunology, University of Melbourne Peter Doherty Institute for Infection and Immunity 792 Elizabeth St, Melbourne 3000, Australia (1)

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Type III Secretion Effectors with Arginine N-Glycosyltransferase Activity.

Not available

S-EPMC7142665 | biostudies-literature

An O-glycosyltransferase promotes cell adhesion during development by influencing secretion of an extracellular matrix integrin ligand.

Not available

S-EPMC2885228 | biostudies-literature

A structural basis for the strain-dependent UDP-sugar specificity of glycosyltransferase C from the Limosilactobacillus reuteri accessory secretion system.

Not available

S-EPMC12809243 | biostudies-literature

New Helical Binding Domain Mediates a Glycosyltransferase Activity of a Bifunctional Protein.

Not available

S-EPMC5063993 | biostudies-literature

NleB host targets - The bacterial arginine glycosyltransferase effector NleB preferentially modifies Fas-associated death domain protein (FADD)

The inhibition of host innate immunity pathways is essential for the survival of attaching and effacing (A/E) pathogens such as enteropathogenic Escherichia coli (EPEC) and Citrobacter rodentium during mammalian infections. To subvert these pathways, A/E pathogens utilize a type III secretion system...

ORGANISM(S): Homo sapiens (Human) Mus musculus (Mouse) Escherichia coli

2017-09-11 | PXD006810 | Pride