The chemical compound 5-methyluridine (symbol m5U), also called ribothymidine (rT), is a pyrimidine nucleoside. It is the ribonucleoside counterpart to the deoxyribonucleoside thymidine, which lacks a hydroxyl group at the 2' position. 5-Methyluridine contains a thymine base joined to a ribose pentose sugar. It is a white solid.
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| IUPAC name 5-Methyluridine | |
| Systematic IUPAC name 1-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4(1H,3H)-dione | |
| Other names Ribothymidine, Ribosylthymine; Thymine riboside, m5U | |
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| ECHA InfoCard | 100.014.522 |
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| Properties | |
| C10H14N2O6 | |
| Molar mass | 258.23 g/mol |
| Density | 1,6 g/cm3 |
| Melting point | 184 °C (363 °F; 457 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references | |
m5U is one of the most common modifications made to cellular RNA. It almost universally occurs in position 54 (part of the T arm) of eukaryotic and bacterial tRNA, serving to stabilize the molecule. The same "T-loop" motif occurs in many other forms of noncoding RNA such as tmRNA and rRNA. Loss of the tRNA modification does not usually produce a different, less fit, phenotype.
See also
- 5-Methylcytosine
- 3-Methyluridine
Footnotes
- The term ribothymidine is especially used to describe its unusual occurrence in RNA.
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