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14 relations: Catabolism, Catalysis, Chemical reaction, Enzyme, Gene, Heparan sulfate, Heparin, Hydrolysis, Keratan sulfate, List of enzymes, Lysosomal storage disease, Lysosome, Mucopolysaccharidosis, Sanfilippo syndrome.
Catabolism
Catabolism (from Greek κάτω kato, "downward" and βάλλειν ballein, "to throw") is the set of metabolic pathways that breaks down molecules into smaller units that are either oxidized to release energy or used in other anabolic reactions.
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Catalysis
Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.
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Chemical reaction
A chemical reaction is a process that leads to the transformation of one set of chemical substances to another.
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Enzyme
Enzymes are macromolecular biological catalysts.
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Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
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Heparan sulfate
Heparan sulfate (HS) is a linear polysaccharide found in all animal tissues.
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Heparin
Heparin, also known as unfractionated heparin (UFH), is medication which is used as an anticoagulant (blood thinner).
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Hydrolysis
Hydrolysis is a term used for both an electro-chemical process and a biological one.
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Keratan sulfate
Keratan sulfate (KS), also called keratosulfate, is any of several sulfated glycosaminoglycans (structural carbohydrates) that have been found especially in the cornea, cartilage, and bone.
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List of enzymes
This page lists enzymes by their classification in the International Union of Biochemistry and Molecular Biology's Enzyme Commission numbering system.
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Lysosomal storage disease
Lysosomal storage diseases (LSDs) are a group of about 50 rare inherited metabolic disorders that result from defects in lysosomal function.
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Lysosome
A lysosome is a membrane-bound organelle found in nearly all animal cells.
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Mucopolysaccharidosis
Mucopolysaccharidoses are a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called glycosaminoglycans.
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Sanfilippo syndrome
Sanfilippo syndrome, or mucopolysaccharidosis III (MPS-III) is a rare autosomal recessive lysosomal storage disease.
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Redirects here:
2-acetamido-2-deoxy-D-glucose 6-sulfate sulfatase, Acetylglucosamine 6-sulfatase, Acetylglucosamine sulfatase, EC 3.1.6.14, GNS (gene), GNS Gene, GNS gene, N-acetyl-D-glucosamine-6-sulfate 6-sulfohydrolase, N-acetylglucosamine 6-sulfatase, N-acetylglucosamine 6-sulfate sulfatase, N-acetylglucosamine-G-sulfate sulfatase, O,N-disulfate O-sulfohydrolase.
References
[1] https://en.wikipedia.org/wiki/N-acetylglucosamine-6-sulfatase
