Choline-sulfatase

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choline-sulfatase
Identifiers
EC no. 3.1.6.6
CAS no. 9025-59-6
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MetaCyc metabolic pathway
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The enzyme choline-sulfatase (EC 3.1.6.6) [1] catalyzes the reaction

choline sulfate + H2O choline + sulfate

This enzyme belongs to the family of hydrolases, specifically those acting on sulfuric ester bonds. The systematic name is choline-sulfate sulfohydrolase.

Related Research Articles

<span class="mw-page-title-main">X-linked ichthyosis</span> Medical condition

X-linked ichthyosis is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000 to 1 in 6000 males. XLI manifests with dry, scaly skin and is due to deletions or mutations in the STS gene. XLI can also occur in the context of larger deletions causing contiguous gene syndromes. Treatment is largely aimed at alleviating the skin symptoms. The term is from the Ancient Greek 'ichthys' meaning 'fish'.

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<span class="mw-page-title-main">Sulfatase</span> Class of enzymes

Sulfatases EC 3.1.6.- are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates.

<span class="mw-page-title-main">Arylsulfatase B</span> Mammalian protein found in Homo sapiens

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<span class="mw-page-title-main">Arylsulfatase</span>

Arylsulfatase (EC 3.1.6.1, sulfatase, nitrocatechol sulfatase, phenolsulfatase, phenylsulfatase, p-nitrophenyl sulfatase, arylsulfohydrolase, 4-methylumbelliferyl sulfatase, estrogen sulfatase) is a type of sulfatase enzyme with systematic name aryl-sulfate sulfohydrolase. This enzyme catalyses the following chemical reaction

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N-acetylgalactosamine-6-sulfatase is an enzyme that, in humans, is encoded by the GALNS gene.

<span class="mw-page-title-main">N-acetylglucosamine-6-sulfatase</span> Protein-coding gene in the species Homo sapiens

N-acetylglucosamine-6-sulfatase (EC 3.1.6.14, glucosamine (N-acetyl)-6-sulfatase, systematic name N-acetyl-D-glucosamine-6-sulfate 6-sulfohydrolase) is an enzyme that in humans is encoded by the GNS gene. It is deficient in Sanfilippo Syndrome type IIId. It catalyses the hydrolysis of the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of heparan sulfate and keratan sulfate

In enzymology, a choline sulfotransferase is an enzyme that catalyzes the chemical reaction

Estrone sulfotransferase (EST), also known as estrogen sulfotransferase, is an enzyme that catalyzes the transformation of an unconjugated estrogen like estrone into a sulfated estrogen like estrone sulfate. It is a steroid sulfotransferase and belongs to the family of transferases, to be specific, the sulfotransferases, which transfer sulfur-containing groups. This enzyme participates in androgen and estrogen metabolism and sulfur metabolism.

<span class="mw-page-title-main">N-sulfoglucosamine sulfohydrolase</span>

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In enzymology, a phosphoadenylylsulfatase (EC 3.6.2.2) is an enzyme that catalyzes the chemical reaction

The enzyme chondro-4-sulfatase (EC 3.1.6.9) catalyzes the reaction

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In enzymology, a galactose-6-sulfurylase is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">SUMF1</span> Protein-coding gene in the species Homo sapiens

Sulfatase-modifying factor 1 is an enzyme that in humans is encoded by the SUMF1 gene.

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References

  1. Takebe I (September 1961). "Isolation and characterization of a new enzyme choline sulfatase". Journal of Biochemistry. 50 (3): 245–55. PMID   13919191.