Xanthosine monophosphate
Names | |
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IUPAC name
5'-xanthylic acid
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Other names
xanthine ribotide,
XMP | |
Identifiers | |
3D model (
JSmol ) |
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ChEBI | |
ChemSpider | |
KEGG | |
MeSH | Xanthosine+monophosphate |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H13N4O9P | |
Molar mass | 364.206 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Xanthosine monophosphate (xanthylate) is an intermediate in
IMP dehydrogenase, and it forms GMP via the action of GMP synthase. Also, XMP can be released from XTP by enzyme deoxyribonucleoside triphosphate pyrophosphohydrolase containing (d)XTPase activity.[2]
It is abbreviated XMP.[3]
See also
References
- ISBN 9780495015253. Retrieved 26 March 2012.
- PMID 22531138.
- PMID 21486037.
Further reading
- Sigel, H; Operschall, BP; Griesser, R (2009). "Xanthosine 5'-monophosphate (XMP). Acid-base and metal ion-binding properties of a chameleon-like nucleotide" (PDF). Chemical Society Reviews. 38 (8): 2465–94. S2CID 205726340. Archived from the original(PDF) on 2020-01-01.
- Egli, M; Pallan, PS (2010). "Crystallographic studies of chemically modified nucleic acids: A backward glance". Chemistry & Biodiversity. 7 (1): 60–89. PMID 20087997.