Target intelligence / Profile preview

Arylsulfatase H (ARSH)

Target
ARSH
Molecular classification
Enzyme, Sulfatase, Lysosomal enzyme
01

Overview

Arylsulfatase H (ARSH) is a member of the sulfatase enzyme family, specifically classified as an arylsulfatase, which catalyzes the hydrolysis of sulfate esters from a diverse array of substrates including sulfated steroids, carbohydrates, proteoglycans, and glycolipids[5]. Sulfatase enzymes play crucial roles in regulating hormone metabolism, carbohydrate catabolism, and the degradation of complex molecules involved in cellular and developmental signaling. ARSH, like other sulfatases, is functionally important in lysosomal metabolism, participating in the breakdown of sulfated compounds to maintain cellular homeostasis. While other sulfatases such as arylsulfatase A (ARSA) are directly linked to inherited lysosomal storage diseases, there are currently no well-established disease linkages or clinical biomarker applications described specifically for ARSH. ARSH is considered a therapeutic target due to its classified role as a lysosomal enzyme, but as of now, there are no drugs known to target ARSH directly[5].

Other names
Arylsulfatase HARSHASHsulfatasearylsulfatase H
02

Mechanism of action

Catalytic hydrolysis of sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids[5]

03

Biological functions

Hydrolysis of sulfate estersHormone metabolismCarbohydrate metabolismGlycolipid and proteoglycan degradation
04

Disease associations

Lysosomal storage disorder (general, not directly implicated with a specific disorder as ARSH, but the sulfatase family has this association)

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