- In biochemistry,
sulfatases EC 3.1.6.- are a
class of
enzymes of the
esterase class that
catalyze the
hydrolysis of
sulfate esters into an
alcohol and...
-
Iduronate 2-
sulfatase (EC 3.1.6.13;
systematic name L-iduronate-2-sulfate 2-sulfohydrolase) is a
sulfatase enzyme ****ociated with
Hunter syndrome. It catalyses...
-
syndrome is
caused by a
deficiency of the
lysosomal enzyme iduronate-2-
sulfatase (I2S). The lack of this
enzyme causes heparan sulfate and
dermatan sulfate...
-
Steroid sulfatase (STS), or steryl-
sulfatase (EC 3.1.6.2),
formerly known as
arylsulfatase C, is a
sulfatase enzyme involved in the
metabolism of steroids...
-
Multiple sulfatase deficiency (MSD), also
known as
Austin disease, or mucosulfatidosis, is a very rare
autosomal recessive: 561
lysosomal storage disease...
- is a skin
condition caused by the
hereditary deficiency of the
steroid sulfatase (STS)
enzyme that
affects 1 in 2000 to 1 in 6000 males. XLI manifests...
- N-acetylglucosamine-6-
sulfatase (EC 3.1.6.14,
glucosamine (N-acetyl)-6-
sulfatase,
systematic name N-acetyl-D-glucosamine-6-sulfate 6-sulfohydrolase) is...
-
sulfatase,
nitrocatechol sulfatase, phenolsulfatase, phenylsulfatase, p-nitrophenyl
sulfatase, arylsulfohydrolase, 4-methylumbelliferyl
sulfatase, estrogen...
- MPS II,
Hunter syndrome or
iduronate sulfatase deficiency, is
caused by lack of the
enzyme iduronate sulfatase.
Hunter syndrome has two
clinical subtypes...
- N-acetylgalactosamine-4-
sulfatase (EC 3.1.6.12, chondroitinsulfatase, chondroitinase,
arylsulfatase B,
acetylgalactosamine 4-
sulfatase, N-acetylgalactosamine...
