Structured Summary
Abstract
Enzymes that catalyze the hydrolysis of a phenol sulfate to yield a phenol and sulfate. Arylsulfatase A, B, and C have been separated. A deficiency of arylsulfatases is one of the causes of metachromatic leukodystrophy (LEUKODYSTROPHY, METACHROMATIC). EC 3.1.6.1.
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Classification
Broader headings
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Synonyms
7 entry terms
- Arylsulfatase
- Arylsulfate Sulfohydrolase
- Arylsulfate Sulfohydrolases
- Arylsulphatase
- Arylsulphatases
- Sulfohydrolase, Arylsulfate
- Pseudo Arylsulfatase A
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
91(75); was see under SULFATASES 1975-90
MeSH Record
Previous Indexing
- Phenols (1973-1974)
- Sulfatases (1973-1974)
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AMA Style
References
- National Library of Medicine. Arylsulfatases. Medical Subject Headings (MeSH). 2026. Unique ID D001192. http://id.nlm.nih.gov/mesh/2026/D001192
- Arylsulfatases. In: Wikipedia. https://en.wikipedia.org/wiki/Arylsulfatase
- Arylsulfatases. In: Wikidata. https://www.wikidata.org/wiki/Q4802708