The activation of arylsulfatases

Summary
Organism
Homo sapiens (human)
Reactome
R-HSA-1663150
PubChem
R-HSA-1663150
Description
  • Sulfatase activity requires a unique posttranslational modification (PTM) of a catalytic cysteine residue into a formylglycine. This modification is impaired in patients with multiple sulfatase deficiency (MSD) due to defects in the SUMF1 (sulfatase-modifying factor 1) gene responsible for this PTM. SUMF2 can inhibit the activity of SUMF1 thereby providing a mechanism for the regulation of sulfatase activation (Ghosh 2007, Diez-Roux & Ballabio 2005).
Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
Displaying entries 1 - 10 of 12 in total
UniProt ID Protein Name Gene Symbol Pathway Viewer
P08842 Steryl-sulfatase
  • ARSC1
  • STS
view
P15289 Arylsulfatase A
  • ARSA
view
P15848 Arylsulfatase B
  • ARSB
view
P51689 Arylsulfatase D
  • ARSD
view
P51690 Arylsulfatase L
  • ARSE
  • ARSL
view
P54793 Arylsulfatase F
  • ARSF
view
Q5FYB0 Arylsulfatase J
  • ARSJ
  • UNQ372/PRO708
view
Q5FYB1 Arylsulfatase I
  • ARSI
view
Q6UWY0 Arylsulfatase K
  • ARSK
  • TSULF
  • UNQ630/PRO1246
view
Q8NBJ7 Inactive C-alpha-formylglycine-generating enzyme 2
  • PSEC0171
  • SUMF2
  • UNQ1968/PRO4500
view

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026