Abstract
Background: Human sulfatases play key roles in physiology and cause numerous pathological conditions upon deficiency/misregulation. Results: ARSK is ubiquitously expressed, localizes to lysosomes, and shows arylsulfatase activity at acidic pH. Conclusion: ARSK is a novel lysosomal sulfatase acting on a ubiquitous substrate. Significance: ARSK functions in lysosomal degradation, possibly of glycosaminoglycans, and, in all probability, is associated with a non-classified lysosomal storage disorder. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Wiegmann, E. M., Westendorf, E., Kalus, I., Pringle, T. H., Lübke, T., & Dierks, T. (2013). Arylsulfatase K, a novel lysosomal sulfatase. Journal of Biological Chemistry, 288(42), 30019–30028. https://doi.org/10.1074/jbc.M113.499541
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