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5.1.3.7: UDP-N-acetylglucosamine 4-epimerase

This is an abbreviated version!
For detailed information about UDP-N-acetylglucosamine 4-epimerase, go to the full flat file.

Word Map on EC 5.1.3.7

Reaction

UDP-N-acetyl-alpha-D-glucosamine
=
UDP-N-acetyl-alpha-D-galactosamine

Synonyms

Epimerase, uridine diphosphoacetylglucosamine, Galactowaldenase, GalE, galE-2, GalESp2, GNE, Gne epimerase, group 3 epimerase, KfoA, More, TM0509, TMGalE, UAE, UDP acetylglucosamine epimerase, UDP-galactose 4-epimerase, UDP-galactose-4-epimerase, UDP-GalNAc 4-epimerase, UDP-Glc(NAc) 4-epimerase, UDP-GlcNAc 4-epimerase, UDP-GlcNAc epimerase, UDP-GlcNAc/Glc 4-epimerase, UDP-hexose 4-epimerase, UDP-N-acetylglucosamine 4'-epimerase, UDP-N-acetylglucosamine 4-epimerase, UDP-N-acetylglucosamine-4'-epimerase, UDP-sugar 4-epimerase, UDPGlcNAc 4-epimerase, Uridine 5'-diphospho-N-acetylglucosamine-4-epimerase, Uridine diphosphate N-acetylglucosamine-4-epimerase, Uridine diphosphoacetylglucosamine epimerase, WbgU, WbPP

ECTree

     5 Isomerases
         5.1 Racemases and epimerases
             5.1.3 Acting on carbohydrates and derivatives
                5.1.3.7 UDP-N-acetylglucosamine 4-epimerase

Expression

Expression on EC 5.1.3.7 - UDP-N-acetylglucosamine 4-epimerase

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EXPRESSION
ORGANISM
UNIPROT
LITERATURE
GALE mRNA expression is stimulated by interleukin-1beta in early phase, but suppressed in late phase, while the suppression of GALE expression induced by interleukin-1beta is mainly mediated by stress-activated protein kinase/c-Jun N-terminal kinase pathway
GALE mRNA expression is stimulated by interleukin-1beta in early phase, but suppressed in late phase, while the suppression of GALE expression induced by interleukin-1beta is mainly mediated by stress-activated protein kinase/c-Jun N-terminal kinase pathway. Both SAP/JNK inhibitor SP600125 and p38 MAPK inhibitor SB203580 attenuate the suppression of interleukin-1beta on GAG synthesis and GALE mRNA expression of chondrocyte
overexpression in Thermus thermophilus HB27 leads to an increased capacity of biofilm production
-
spores produced by a mutant strain lacking the enzyme still contain normal levels of BclA-attached oligosaccharides, monosaccharide analysis of the oligosaccharides reveals that N-acetylglucosamine had replaced N-acetylgalactosamine, significant levels of gene transcripts are detected only during sporulation, an observation consistent with a role for this gene in exosporium assembly, gene expression during sporulation appears to be biphasic
Q81JK4