A nucleobase analogue that is cytosine in which the hydrogen at position 5 is replaced by a carboxy group.
Chemical formula | Net charge | Average mass |
---|---|---|
C5H5N3O3 | 0 | 155.11150 |
Name | 5-carboxylcytosine |
---|---|
Abbreviation | 5caC |
Symbol | c |
Complement | guanine:5-carboxylcytosine |
Symbol | 4 |
IUPAC | SMILES | InChI | InChIKey | Synonyms |
---|---|---|---|---|
4-amino-2-oxo-1,2-dihydropyrimidine-5-carboxylic acid | Nc1nc(=O)[nH]cc1C(O)=O | InChI=1S/C5H5N3O3/c6-3-2(4(9)10)1-7-5(11)8-3/h1H,(H,9,10)(H3,6,7,8,11) | BLQMCTXZEMGOJM-UHFFFAOYSA-N |
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Method |
Method detail
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Resolution
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Qualifier
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References |
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CAB-seq | chemical conversion | single-base |
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MAB-seq | chemical conversion | single-base | low-input or single-cell |
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caMAB-seq | chemical conversion | single-base |
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nanopore | direct detection | single-base | target sequences |
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Origin | Function | Functional detail |
Organisms
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References |
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natural | demethylation intermediate and possible epigenetic mark |
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