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5.4.2.3: phosphoacetylglucosamine mutase

This is an abbreviated version!
For detailed information about phosphoacetylglucosamine mutase, go to the full flat file.

Word Map on EC 5.4.2.3

Reaction

N-acetyl-alpha-D-glucosamine 1-phosphate
=
N-acetyl-D-glucosamine 6-phosphate

Synonyms

2-Acetamido-2-deoxy-D-glucose-1,6-bisphosphate:2-acetamido-2-deoxy-D-glucose 1-phosphate phosphotransferase, Acetylaminodeoxyglucose phosphomutase, Acetylglucosamine phosphomutase, AGM, AGM1, AGM1/PGM3, CaAGM1, DNA-damage-repair/toleration protein DRT101, EC 2.7.5.2, EC 2.7.5.2., HsAGM1, N-acetylglucosamine-phosphate mutase, PAGM, PGlcNAc mutase, PGM3, Phospho-N-acetylglucosamine mutase, phosphoacetylglucosamine mutase 1, Phosphomutase, acetylglucosamine

ECTree

     5 Isomerases
         5.4 Intramolecular transferases
             5.4.2 Phosphotransferases (phosphomutases)
                5.4.2.3 phosphoacetylglucosamine mutase

General Information

General Information on EC 5.4.2.3 - phosphoacetylglucosamine mutase

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GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
evolution
malfunction
loss-of-function mutations in the nst gene, which encodes PGM3, block fibroblast growth factor signaling during embryonic mesoderm and tracheal development. In nst mutants with an 80% reduction in the amount of UDP-GlcNAc, O-GlcNAcylation is compromised. Embryos maternally and zygotically mutant for nst exhibit defects in mesoderm layer formation during gastrulation that are similar to those observed in embryos with mutations in the gene encoding the fibroblast growth factor receptor Heartless (Htl). Zygotic nst mutants (nstZ) exhibit normal dorsal mesoderm differentiation, embryos homozygous for the hypomorphic htlYY262 allele show a reduction in dorsal mesoderm. Phenotypes, overview. Dof is the critical component in MAPK activation affected in nst mutants
metabolism
Nst acts downstream of fibroblast growth factor receptor signaling
physiological function