Coenzyme A | |
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Identifiers | |
CAS number | 85-61-0 |
PubChem | 6816 |
ChemSpider | 6557 |
UNII | SAA04E81UX |
DrugBank | DB01992 |
KEGG | C00010 |
MeSH | Coenzyme+A |
ChEMBL | CHEMBL1213327 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C21H36N7O16P3S |
Molar mass | 767.535 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Coenzyme A (CoA, CoASH, or HSCoA) is a coenzyme, notable for its role in the synthesis and oxidation of fatty acids, and the oxidation of pyruvate in the citric acid cycle. All sequenced genomes encode enzymes that use coenzyme A as a substrate, and around 4% of cellular enzymes use it (or a thioester, such as acetyl-CoA) as a substrate.[1] It is adapted from cysteamine, pantothenate, and adenosine triphosphate.
Contents |
Coenzyme A is synthesized in a five-step process from pantothenate and cysteine:
Since coenzyme A is, in chemical terms, a thiol, it can react with carboxylic acids to form thioesters, thus functioning as an acyl group carrier. It assists in transferring fatty acids from the cytoplasm to mitochondria. A molecule of coenzyme A carrying an acetyl group is also referred to as acetyl-CoA. When it is not attached to an acyl group, it is usually referred to as 'CoASH' or 'HSCoA'.
Coenzyme A is also the source of the phosphopantetheine group that is added as a prosthetic group to proteins such as acyl carrier protein and formyltetrahydrofolate dehydrogenase.[2][3]
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