- with sulfotransferases,
sulfatases form the
major catalytic machinery for the
synthesis and
breakage of
sulfate esters.
Sulfatases are
found in
lower and...
-
caused by a
deficiency in
multiple sulfatase enzymes, or in formylglycine-generating enzyme,
which activates sulfatases.: 502 It is
similar to mucopolysaccharidosis...
-
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...
- 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...
-
sulfatase,
nitrocatechol sulfatase, phenolsulfatase, phenylsulfatase, p-nitrophenyl
sulfatase, arylsulfohydrolase, 4-methylumbelliferyl
sulfatase, estrogen...
- anaerobic. FGE
activates sulfatases,
which are
essential for the
degradation of
sulfate esters. The
catalytic activity of
sulfatases is
dependent upon a formylglycine...
-
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...
-
hydrolases may be nucleases, proteases, glycosidases, lipases, phosphatases,
sulfatases and
phospholipases and make up the
approximately 50
degradative enzymes...
-
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...
- MPS IV
Morquio syndrome type Gene
Missing enzyme Chromosomal region Type A
GALNS Galactosamine-6
sulfatase 16q24 Type B GLB1 Beta-galactosidase 3p22...
