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Arylsulfatase A

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Arylsulfatase A (or cerebroside-sulfatase) is an enzyme that breaks down sulfatides, namely cerebroside 3-sulfate into cerebroside and sulfate. In humans, arylsulfatase A is encoded by the ARSA gene.[5][6]

AliasesARSA, MLD, arylsulfatase A, ASA
External IDsOMIM: 607574; MGI: 88077; GeneCards: ARSA
PDBOrtholog search: PDBe RCSB
Quick facts ARSA, Identifiers ...
ARSA
Identifiers
AliasesARSA, MLD, arylsulfatase A, ASA
External IDsOMIM: 607574; MGI: 88077; GeneCards: ARSA
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
3.1.6.8↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_009713

RefSeq (protein)

NP_033843

Location (UCSC)Chr 22: 50.62 – 50.63 MbChr 15: 89.36 – 89.36 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

A deficiency in Arylsulfatase A is associated with metachromatic leukodystrophy, an autosomal recessive disease.[7] Multiple sulfatase deficiency (MSD) is also associated with the ARSA gene.[8]

Biochemistry

Enzyme regulation

Arylsulfatase A is inhibited by phosphate, which forms a covalent bond with the active site 3-oxoalanine.[9]

References

Further reading

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