Aryl-sulfate sulfotransferase

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arylsulfate sulfotransferase
Identifiers
EC no. 2.8.2.22
CAS no. 158254-86-5
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MetaCyc metabolic pathway
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In enzymology, an aryl-sulfate sulfotransferase (EC 2.8.2.22) is an enzyme that catalyzes the chemical reaction

an aryl sulfate + a phenol a phenol + an aryl sulfate

Thus, the two substrates of this enzyme are aryl sulfate and phenol, whereas its two products are phenol and aryl sulfate.

This enzyme belongs to the family of transferases, specifically the sulfotransferases, which transfer sulfur-containing groups. The systematic name of this enzyme class is aryl-sulfate:phenol sulfotransferase. Other names in common use include arylsulfate-phenol sulfotransferase, arylsulfotransferase, ASST, arylsulfate sulfotransferase, and arylsulfate:phenol sulfotransferase.

See also

Related Research Articles

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<span class="mw-page-title-main">SULT1A1</span> Protein-coding gene in the species Homo sapiens

Sulfotransferase 1A1 is an enzyme that in humans is encoded by the SULT1A1 gene.

<span class="mw-page-title-main">SULT1A2</span> Protein-coding gene in the species Homo sapiens

Sulfotransferase 1A2 is an enzyme that in humans is encoded by the SULT1A2 gene.

<span class="mw-page-title-main">SULT1C2</span> Protein-coding gene in the species Homo sapiens

Sulfotransferase 1C2 is an enzyme that in humans is encoded by the SULT1C2 gene.

Phenol sulfur transferase deficiency, in short PST deficiency, is the lack or the reduced activity of the functional enzyme phenol sulfur transferase, which is crucial in the detoxification of mainly phenolic compounds by catalysing the sulfate conjugation of the hydroxyl groups in the toxic phenolic compounds to result in more hydrophilic forms for more efficient excretion. This metabolic disorder was first discovered in the late 1990s by Dr. Rosemary Waring during her researches with autistic children, which also made this deficiency commonly associated to the topics of autism. Mutations in the PST genes account for the genetic causes of the deficiency, of which single nucleotide polymorphism and methylation of promoters are two examples of mutations that respectively cause conformational abnormalities and diminished expressions to the enzyme, resulting in the reduced detoxification of phenolic compounds and regulation of phenolic neurotransmitter. The deficiency may cause symptoms like flushing, tachycardia, and depression, and be a risk factor for disorders like autism, migraine, and cancer, while it also limits the use of phenolic drugs in PST deficient patients. There is currently no drug available for treating PST deficiency. However, some people suffering from PST deficiency have found taking a digestive enzyme supplement containing Xylanase 10 minutes before eating to greatly reduce symptoms.

References