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arylsulfatase E-like [Loxodonta africana]
Sulfatase_C domain-containing protein( domain architecture ID 10631472)
Sulfatase_C domain-containing protein
List of domain hits
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Name | Accession | Description | Interval | E-value | |||
Sulfatase_C | pfam14707 | C-terminal region of aryl-sulfatase; |
1-129 | 2.82e-53 | |||
C-terminal region of aryl-sulfatase; : Pssm-ID: 405407 [Multi-domain] Cd Length: 122 Bit Score: 163.64 E-value: 2.82e-53
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Name | Accession | Description | Interval | E-value | |||
Sulfatase_C | pfam14707 | C-terminal region of aryl-sulfatase; |
1-129 | 2.82e-53 | |||
C-terminal region of aryl-sulfatase; Pssm-ID: 405407 [Multi-domain] Cd Length: 122 Bit Score: 163.64 E-value: 2.82e-53
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ES | cd16159 | Estrone sulfatase; Human estrone sulfatase (ES) is responsible for maintaining high levels of ... |
2-107 | 1.10e-43 | |||
Estrone sulfatase; Human estrone sulfatase (ES) is responsible for maintaining high levels of the active estrogen in tumor cells. ES catalyzes the hydrolysis of E1 sulfate, which is a component of the three-enzyme system that has been implicated in intracrine biosynthesis of estradiol. It is associated with the membrane of the endoplasmic reticulum (ER). The structure of ES consisting of two antiparallel alpha helices that protrude from the roughly spherical molecule. These highly hydrophobic helices anchor the functional domain on the membrane surface facing the ER lumen. Pssm-ID: 293778 [Multi-domain] Cd Length: 521 Bit Score: 149.75 E-value: 1.10e-43
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Name | Accession | Description | Interval | E-value | |||
Sulfatase_C | pfam14707 | C-terminal region of aryl-sulfatase; |
1-129 | 2.82e-53 | |||
C-terminal region of aryl-sulfatase; Pssm-ID: 405407 [Multi-domain] Cd Length: 122 Bit Score: 163.64 E-value: 2.82e-53
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ES | cd16159 | Estrone sulfatase; Human estrone sulfatase (ES) is responsible for maintaining high levels of ... |
2-107 | 1.10e-43 | |||
Estrone sulfatase; Human estrone sulfatase (ES) is responsible for maintaining high levels of the active estrogen in tumor cells. ES catalyzes the hydrolysis of E1 sulfate, which is a component of the three-enzyme system that has been implicated in intracrine biosynthesis of estradiol. It is associated with the membrane of the endoplasmic reticulum (ER). The structure of ES consisting of two antiparallel alpha helices that protrude from the roughly spherical molecule. These highly hydrophobic helices anchor the functional domain on the membrane surface facing the ER lumen. Pssm-ID: 293778 [Multi-domain] Cd Length: 521 Bit Score: 149.75 E-value: 1.10e-43
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GALNS | cd16157 | galactosamine-6-sulfatase; also known as N-acetylgalactosamine-6-sulfatase (GALNS); Lysosomal ... |
54-107 | 4.03e-10 | |||
galactosamine-6-sulfatase; also known as N-acetylgalactosamine-6-sulfatase (GALNS); Lysosomal galactosamine-6-sulfatase removes sulfate groups from a terminal N-acetylgalactosamine-6-sulfate (or galactose-6-sulfate) in mucopolysaccharides such as keratan sulfate and chondroitin-6-sulfate. Defects in GALNS lead to accumulation of substrates, resulting in the development of the lysosomal storage disease mucopolysaccharidosis IV A. Pssm-ID: 293776 [Multi-domain] Cd Length: 466 Bit Score: 56.32 E-value: 4.03e-10
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spARS_like | cd16160 | sea urchin arylsulfatase-like; This family includes sea urchin arylsulfatase and its ... |
3-88 | 7.83e-10 | |||
sea urchin arylsulfatase-like; This family includes sea urchin arylsulfatase and its homologous proteins. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases. Pssm-ID: 293779 [Multi-domain] Cd Length: 445 Bit Score: 55.51 E-value: 7.83e-10
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ARSA | cd16158 | Arylsulfatase A or cerebroside-sulfatase; Arylsulfatase A breaks down sulfatides, namely ... |
10-121 | 1.81e-07 | |||
Arylsulfatase A or cerebroside-sulfatase; Arylsulfatase A breaks down sulfatides, namely cerebroside 3-sulfate into cerebroside and sulfate. It is a member of the sulfatase family. The arylsulfatase A was located in lysosome-like structures and transported to dense lysosomes in a mannose 6-phosphate receptor-dependent manner. Deficiency of arylsulfatase A leads to the accumulation of cerebroside sulfate, which causes a lethal progressive demyelination. Arylsulfatase A requires the posttranslational oxidation of the -CH2SH group of a conserved cysteine to an aldehyde, yielding a formylglycine to be in an active form. Pssm-ID: 293777 [Multi-domain] Cd Length: 479 Bit Score: 48.60 E-value: 1.81e-07
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GALNS_like | cd16026 | galactosamine-6-sulfatase; also known as N-acetylgalactosamine-6-sulfatase (GALNS); Lysosomal ... |
2-74 | 3.38e-06 | |||
galactosamine-6-sulfatase; also known as N-acetylgalactosamine-6-sulfatase (GALNS); Lysosomal galactosamine-6-sulfatase removes sulfate groups from a terminal N-acetylgalactosamine-6-sulfate (or galactose-6-sulfate) in mucopolysaccharides such as keratan sulfate and chondroitin-6-sulfate. Defects in GALNS lead to accumulation of substrates, resulting in the development of the lysosomal storage disease mucopolysaccharidosis IV A. Pssm-ID: 293750 [Multi-domain] Cd Length: 399 Bit Score: 44.86 E-value: 3.38e-06
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ARSG | cd16161 | arylsulfatase G; Arylsulfatase G is a subfamily of sulfatases which specifically hydrolyze ... |
22-74 | 8.20e-05 | |||
arylsulfatase G; Arylsulfatase G is a subfamily of sulfatases which specifically hydrolyze sulfate esters in a wide variety of substrates such as glycosaminoglycans, steroid sulfates, or sulfolipids. ARSG has arylsulfatase activity toward different pseudosubstrates like p-nitrocatechol sulfate and 4-methylumbelliferyl sulfate. An active site Cys is post-translationally converted to the critical active site C(alpha)-formylglycine. ARSG mRNA expression was found to be tissue-specific with highest expression in liver, kidney, and pancreas, suggesting a metabolic role of ARSG that might be associated with a non-classified lysosomal storage disorder. Pssm-ID: 293780 [Multi-domain] Cd Length: 383 Bit Score: 40.92 E-value: 8.20e-05
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ARS_like | cd16142 | uncharacterized arylsulfatase subfamily; Sulfatases catalyze the hydrolysis of sulfate esters ... |
5-74 | 2.39e-04 | |||
uncharacterized arylsulfatase subfamily; Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases. Pssm-ID: 293761 [Multi-domain] Cd Length: 372 Bit Score: 39.44 E-value: 2.39e-04
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Blast search parameters | ||||
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