Difference between revisions of "Part:BBa K5499002"
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Name: Iduronate-2-sulfatase (IDS)
 
Name: Iduronate-2-sulfatase (IDS)
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Origin: Homo sapiens, synthetic
 
Origin: Homo sapiens, synthetic
  
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Properties: a kind of lysosomal enzyme that can degrade glycosaminoglycans（GAGs）
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Properties: A kind of lysosomal enzyme that can degrade glycosaminoglycans（GAGs）

Revision as of 15:09, 29 September 2024


Iduronate-2-sulfatase (IDS)

Iduronate-2-sulfatase (IDS) is a lysosomal enzyme that splits the sulfate group in the C-2 positions from iduronic acid residues present in the mucopolysaccharides dermatan sulfate and heparan sulfate.

Usage and Biology

A Deficiency in this enzyme results in the accumulation of these glycosaminoglycans in the lysosomes and subsequently leads to the development of Hunter syndrome(or mucopolysaccharidosis type 2 ) in humans. The disorder is inherited as an X-linked recessive disease and has a broad spectrum of clinical phenotypes ranging from mild to severe forms. This heterogeneity has been postulated to reflect the presence of different mutations in the IDS gene.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Profile

Name: Iduronate-2-sulfatase (IDS)

Base Pairs:1650 bp

Origin: Homo sapiens, synthetic

Properties: A kind of lysosomal enzyme that can degrade glycosaminoglycans（GAGs）