4.4 Review Book Chapter

Sulfatases and human disease

Journal

ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
Volume 6, Issue -, Pages 355-379

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.genom.6.080604.162334

Keywords

gene families; posttranslational modification; formylglycine; lysosomes; metabolic diseases

Funding

  1. Telethon [TGM03S01, TGM06S01] Funding Source: Medline

Ask authors/readers for more resources

Sulfatases are a highly conserved family of proteins that cleave sulfate esters from a wide range of substrates. The importance of sulfatases in human metabolism is underscored by the presence of at least eight human monogenic diseases caused by the deficiency of individual sulfatases. Sulfatase activity requires a unique posttranslational modification, which is impaired in patients with multiple sulfatase deficiency (MSD) due to a mutation of the sulfatase modifying factor 1 (SUMF1). Here we review current knowledge and future perspectives on the evolution of the sulfatase gene family, on the role of these enzymes in human metabolism, and on new developments in the therapy of sulfatase deficiencies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available