Descriptor English: | Arylsulfatases | ||||||
Descriptor Spanish: |
Arilsulfatasas
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Descriptor Portuguese: | Arilsulfatases | ||||||
Descriptor French: | Arylsulfatases | ||||||
Entry term(s): |
Arylsulfatase Arylsulfate Sulfohydrolase Arylsulfate Sulfohydrolases Arylsulphatase Arylsulphatases Pseudo Arylsulfatase A Sulfohydrolase, Arylsulfate |
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Tree number(s): |
D08.811.277.352.827.070 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D001192 | ||||||
Scope note: | 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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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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Registry Number: | EC 3.1.6.1 | ||||||
CAS Type 1 Name: | Aryl-sulfate sulfohydrolase | ||||||
Previous Indexing: |
Phenols (1973-1974) Sulfatases (1973-1974) |
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Public MeSH Note: | 91; was see under SULFATASES 1975-90 |
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History Note: | 91(75); was see under SULFATASES 1975-90 |
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DeCS ID: | 1198 | ||||||
Unique ID: | D001192 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1991/01/01 | ||||||
Date of Entry: | 1974/11/19 | ||||||
Revision Date: | 2020/05/27 |
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CHEMICALS AND DRUGS
Enzymes and Coenzymes [D08]Enzymes and Coenzymes
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Arylsulfatases
- Preferred
Pseudo Arylsulfatase A
- Narrower
Concept UI |
M0001780 |
Scope note | 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. |
Preferred term | Arylsulfatases |
Entry term(s) |
Arylsulfatase Arylsulfate Sulfohydrolase Arylsulfate Sulfohydrolases Arylsulphatase Arylsulphatases Sulfohydrolase, Arylsulfate |
Concept UI |
M0001781 |
Preferred term | Pseudo Arylsulfatase A |
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