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Uridine diphosphate N-acetylglucosamine

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Uridine diphosphate N-acetylglucosamine
Names
IUPAC name Uridine 5′-(2-acetamido-2-deoxy-α-D-glucopyranosyl dihydrogen diphosphate)
Systematic IUPAC name O- O-{methyl} dihydrogen diphosphate
Other names UDP-N-acetylglucosamine; UDP-GlcNAc
Identifiers
CAS Number
3D model (JSmol)
IUPHAR/BPS
PubChem CID
CompTox Dashboard (EPA)
SMILES
  • CC(=O)N1(((O1OP(=O)(O)OP(=O)(O)OC2(((O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
Properties
Chemical formula C17H27N3O17P2
Molar mass 607.355 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

Uridine diphosphate N-acetylglucosamine or UDP-GlcNAc is a nucleotide sugar and a coenzyme in metabolism. It is used by glycosyltransferases to transfer N-acetylglucosamine residues to substrates. D-Glucosamine is made naturally in the form of glucosamine-6-phosphate, and is the biochemical precursor of all nitrogen-containing sugars. To be specific, glucosamine-6-phosphate is synthesized from fructose 6-phosphate and glutamine as the first step of the hexosamine biosynthesis pathway. The end-product of this pathway is UDP-GlcNAc, which is then used for making glycosaminoglycans, proteoglycans, and glycolipids.

UDP-GlcNAc is extensively involved in intracellular signaling as a substrate for O-linked N-acetylglucosamine transferases (OGTs) to install the O-GlcNAc post-translational modification in a wide range of species. It is also involved in nuclear pore formation and nuclear signalling. OGTs and OG-ases play an important role in the structure of the cytoskeleton. In mammals, there is enrichment of OGT transcripts in the pancreas beta-cells, and UDP-GlcNAc is thought to be part of the glucose sensing mechanism. There is also evidence that it plays a part in insulin sensitivity in other cells. In plants, it is involved in the control of gibberellin production.

Clostridium novyi type A alpha-toxin is an O-linked N-actetylglucosamine transferase acting on Rho proteins and causing the collapse of the cytoskeleton.

References

  1. Roseman S (2001). "Reflections on glycobiology". The Journal of Biological Chemistry. 276 (45): 41527–42. doi:10.1074/jbc.R100053200. PMID 11553646.
  2. Sudhamoy Ghosh, Blumenthal HJ, Davidson E, Roseman S (1960-05-01). "Glucosamine Metabolism". Journal of Biological Chemistry. 235 (5): 1265–73. doi:10.1016/S0021-9258(18)69397-4. PMID 13827775.
  3. International Union of Biochemistry and Molecular Biology
  4. Milewski S, Gabriel I, Olchowy J (2006). "Enzymes of UDP-GlcNAc biosynthesis in yeast". Yeast. 23 (1): 1–14. doi:10.1002/yea.1337. PMID 16408321.
  5. Hanover JA (2001). "Glycan-dependent signaling: O-linked N-acetylglucosamine". The FASEB Journal. 15 (11): 1865–1876. CiteSeerX 10.1.1.324.6370. doi:10.1096/fj.01-0094rev. PMID 11532966.
Types of nucleotide sugars
Purine receptor modulators
Receptor
(ligands)
P0 (adenine)
P1
(adenosine)
P2
(nucleotide)
P2X
(ATPTooltip Adenosine triphosphate)
P2Y
Transporter
(blockers)
CNTsTooltip Concentrative nucleoside transporters
ENTsTooltip Equilibrative nucleoside transporters
PMATTooltip Plasma membrane monoamine transporter
Enzyme
(inhibitors)
XOTooltip Xanthine oxidase
Others
Others
See also: Receptor/signaling modulators
Categories:
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