Arylsulfatase G

Summary
UniProt ID
Q96EG1
Gene Symbol
  • ARSG
  • KIAA1001
Organism
Homo sapiens (human)
External Links
PubChem
Q96EG1
The Human Metabolome Database
HMDBP07458
Annotation
Keyword
  • Calcium
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Hydrolase
  • Lysosome
  • Metal-binding
  • Reference proteome
  • Retinitis pigmentosa
  • Signal
  • Usher syndrome
Gene Ontology (GO)
Sequence
MGWLFLKVLLAGVSFSGFLYPLVDFCISGKTRGQKPNFVIILADDMGWGDLGANWAETKDTANLDKMASEGMRFVDFHAAASTCSPSRASLLTGRLGLRNGVTRNFAVTSVGGLPLNETTLAEVLQQAGYVTGIIGKWHLGHHGSYHPNFRGFDYYFGIPYSHDMGCTDTPGYNHPPCPACPQGDGPSRNLQRDCYTDVALPLYENLNIVEQPVNLSSLAQKYAEKATQFIQRASTSGRPFLLYVALAHMHVPLPVTQLPAAPRGRSLYGAGLWEMDSLVGQIKDKVDHTVKENTFLWFTGDNGPWAQKCELAGSVGPFTGFWQTRQGGSPAKQTTWEGGHRVPALAYWPGRVPVNVTSTALLSVLDIFPTVVALAQASLPQGRRFDGVDVSEVLFGRSQPGHRVLFHPNSGAAGEFGALQTVRLERYKAFYITGGARACDGSTGPELQHKFPLIFNLEDDTAEAVPLERGGAEYQAVLPEVRKVLADVLQDIANDNISSADYTQDPSVTPCCNPYQIACRCQAA
Glycosylation Sites
Displaying all 4 entries
Position Description PubMed ID GlyTouCan ID Source
117 N-linked (GlcNAc...) asparagine
215 N-linked (GlcNAc...) asparagine
356 N-linked (GlcNAc...) asparagine
497 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 2 entries
Pathway Name Organism
Glycosphingolipid catabolism Homo sapiens
The activation of arylsulfatases Homo sapiens
Disease
Displaying entries 1 - 10 of 56 in total
DO ID Disease Name Source
DOID:83 cataract
DOID:0110828 Usher syndrome type 3
DOID:0050439 Usher syndrome
DOID:0050534 congenital stationary night blindness
DOID:0050753 cerebellar ataxia
DOID:0050835 generalized dystonia
DOID:0050836 focal dystonia
DOID:0050841 focal hand dystonia
DOID:0110720 neuronal ceroid lipofuscinosis 4
DOID:0110721 neuronal ceroid lipofuscinosis 1

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024