Uridine diphosphate N-acetylglucosamine

Uridine diphosphate N-acetylglucosamine
Names
	IUPAC name [(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate
	Other names UDP-N-acetylglucosamine; UDP-GlcNAc
Identifiers
CAS Number	91183-98-1 ;
3D model (JSmol)	Interactive image;
IUPHAR/BPS	1779;
PubChem CID	445675;
CompTox Dashboard (EPA)	DTXSID10912327 ;
	SMILES CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)CO)O)O;
Properties
Chemical formula	C17H27N3O17P2
Molar mass	607.355 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

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.[1] To be specific, glucosamine-6-phosphate is synthesized from fructose 6-phosphate and glutamine[2] as the first step of the hexosamine biosynthesis pathway.[3] The end-product of this pathway is UDP-GlcNAc, which is then used for making glycosaminoglycans, proteoglycans, and glycolipids.[4]

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.[5]

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

Roseman, S (2001). "Reflections on glycobiology". The Journal of Biological Chemistry. 276 (45): 41527–42. doi:10.1074/jbc.R100053200. PMID 11553646.
Sudhamoy Ghosh; Blumenthal, HJ; Davidson, E; Roseman, S (1960-05-01). "Glucosamine Metabolism". Journal of Biological Chemistry. 235 (5): 1265–73. PMID 13827775.
International Union of Biochemistry and Molecular Biology
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.
Hanover, J. A. (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.

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[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. 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, J. A. (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.