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EC Number
Natural Substrates
Commentary (Nat. Sub.)
3.1.6.13
dermatan sulfate + H2O
-
3.1.6.13
heparan sulfate + H2O
-
3.1.6.13
heparin + H2O
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3.1.6.13
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The enzyme has a potential role in normal pathway of lysosomal degradation of secretory peptides and is likely to be essential to maintain pancreatic beta-cell function
3.1.6.13
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the enzyme is involved in the catabolism of the mucopolysaccharides heparan and dermatan sulfate
3.1.6.13
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the enzyme is involved in the sequential degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate
3.1.6.13
more
the enzyme is responsible for heparin sulfate and dermatan sulfate degradation
3.1.6.13
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involved in the degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. An enzyme deficiency causes the lysosomal storage disorder muco-polysaccharidosis type II
3.1.6.13
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mucopolysaccharidosis type II is a lysosomal storage disorder related to a deficiency in the enzyme iduronate-2-sulfatase
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