Xanthosine monophosphate
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(Redirected from Xanthylate)
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| Names | |
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| IUPAC name
5'-xanthylic acid
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| Other names
xanthine ribotide,
XMP | |
| Identifiers | |
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3D model (JSmol)
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| MeSH | Xanthosine+monophosphate |
PubChem CID
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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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Template:Chembox Footer/trackingTemplate:Short description
Xanthosine monophosphate (xanthylate) is an intermediate in purine metabolism.[1] It is a ribonucleoside monophosphate. It is formed from IMP via the action of 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
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- ^ Page Module:Citation/CS1/styles.css has no content.McMurry, John (2007). Organic chemistry: a biological approach. Cengage Learning. pp. 1007–. ISBN 9780495015253. Retrieved 26 March 2012.
- ^ Page Module:Citation/CS1/styles.css has no content.Davies O, Mendes P, Smallbone K, Malys N (2012). "Characterisation of multiple substrate-specific (d)ITP/(d)XTPase and modelling of deaminated purine nucleotide metabolism" (PDF). BMB Reports. 45 (4): 259–64. doi:10.5483/BMBRep.2012.45.4.259. PMID 22531138. Archived from the original (PDF) on 2022-05-06. Retrieved 2019-08-16.
- ^ Page Module:Citation/CS1/styles.css has no content.Gogia, S.; Balaram, H.; Puranik, M. (May 2011). "Hypoxanthine guanine phosphoribosyltransferase distorts the purine ring of nucleotide substrates and perturbs the pKa of bound xanthosine monophosphate". Biochemistry. 50 (19): 4184–93. doi:10.1021/bi102039b. PMID 21486037.
Further reading
- Page Module:Citation/CS1/styles.css has no content.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. doi:10.1039/b902181g. PMID 19623361. S2CID 205726340. Archived from the original (PDF) on 2020-01-01.
- Page Module:Citation/CS1/styles.css has no content.Egli, M; Pallan, PS (2010). "Crystallographic studies of chemically modified nucleic acids: A backward glance". Chemistry & Biodiversity. 7 (1): 60–89. doi:10.1002/cbdv.200900177. PMC 2905155. PMID 20087997.
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