2.3.1.78: heparan-alpha-glucosaminide N-acetyltransferase
This is an abbreviated version!
For detailed information about heparan-alpha-glucosaminide N-acetyltransferase, go to the full flat file.
Word Map on EC 2.3.1.78
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2.3.1.78
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lysosomal
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mucopolysaccharidosis
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sanfilippo
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glycosaminoglycans
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naglu
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alpha-n-acetylglucosaminidase
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medicine
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sulfamidase
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n-acetylglucosamine-6-sulfatase
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splice-site
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facies
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nonsyndromic
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pigmentosa
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analysis
- 2.3.1.78
- lysosomal
- mucopolysaccharidosis
-
sanfilippo
- glycosaminoglycans
- naglu
- alpha-n-acetylglucosaminidase
- medicine
-
sulfamidase
- n-acetylglucosamine-6-sulfatase
-
splice-site
-
facies
-
nonsyndromic
- pigmentosa
- analysis
Reaction
Synonyms
acetyl-CoA:alpha-glucosaminide N-acetyltransferase, acetyl-coenzyme A-alpha-glucosaminide N-acetyltransferase, acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase, acetyl-coenzyme:alpha-D-2-amino-glucosamine transferase, acetyltransferase, alpha-glucosaminide, acetyl–coenzyme A:alpha-glucosaminide N-acetyltransferase, GNAT, heparan sulfate acetyl-CoA: alpha-glucosaminide N-acetyltransferase, heparan sulfate acetyl-CoA:alpha-glucosaminide N-acetyltransferase, HGSNAT, TMEM76, transmembrane protein 76
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Substrates Products
Substrates Products on EC 2.3.1.78 - heparan-alpha-glucosaminide N-acetyltransferase
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REACTION DIAGRAM
acetyl-CoA + 1-[4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionyl-glycylamino]-beta-D-glucosamine
CoA + 1-[4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionyl-glycylamino]-N-acetyl-beta-D-glucosamine
i.e. fluorescent BODIPY-glucosamine
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-
?
acetyl-CoA + 4-methylumbelliferyl beta-D-glucosaminide
?
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substrate activity assay
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-
?
acetyl-CoA + 4-methylumbelliferyl-alpha-D-glucosaminide
CoA + 4-methylumbelliferyl-N-acetyl-alpha-D-glucosaminide
acetyl-CoA + 4-methylumbelliferyl-beta-D-glucosaminide
CoA + 4-methylumbelliferyl-N-acetyl-beta-D-glucosaminide
acetyl-CoA + alpha-D-glucosamine
CoA + N-acetyl-alpha-D-glucosamine
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-
-
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?
acetyl-CoA + BODIPY-beta-D-glucosaminide
CoA + BODIPY-N-acetyl-beta-D-glucosaminide
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-
-
?
acetyl-CoA + glucosamine-L-iduronic acid-D-glucosamine
?
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reduced with NaBH4
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-
?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
acetyl-CoA + heparin alpha-D-glucosaminide
CoA + heparin N-acetyl-D-glucosamine
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also acetylates di- and tetrasaccharide fragments of heparin
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-
?
acetyl-CoA + phosphatidylethanolamine
CoA + N-acetylphosphatidylethanolamine
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-
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?
CoA + 4-methylumbelliferyl-N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + 4-methylumbelliferyl-alpha-D-glucosaminide
CoA + 4-methylumbelliferyl-N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + 4-methylumbelliferyl-alpha-D-glucosaminide
CoA + 4-methylumbelliferyl-N-acetyl-alpha-D-glucosaminide
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-
-
?
CoA + 4-methylumbelliferyl-N-acetyl-beta-D-glucosaminide
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?
acetyl-CoA + 4-methylumbelliferyl-beta-D-glucosaminide
CoA + 4-methylumbelliferyl-N-acetyl-beta-D-glucosaminide
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-
-
?
CoA + N-acetyl-beta-D-glucosamine
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-
-
?
acetyl-CoA + beta-D-glucosamine
CoA + N-acetyl-beta-D-glucosamine
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-
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?
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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initial step in heparan sulfate degradation
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
mucopolysaccharidosis IIIC (MPS IIIC, or Sanfilippo C syndrome) is a lysosomal storage disorder caused by the inherited deficiency of the lysosomal membrane enzyme acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase, which leads to impaired degradation of heparan sulfate. Structural protein that transports the activated acetyl residues across the cell membrane
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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-
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
mucopolysaccharidosis IIIC (MPS IIIC, or Sanfilippo C syndrome) is a lysosomal storage disorder caused by the inherited deficiency of the lysosomal membrane enzyme acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase, which leads to impaired degradation of heparan sulfate. Structural protein that transports the activated acetyl residues across the cell membrane
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-
?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
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?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
-
brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed
-
?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
-
brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed
-
?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
-
brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed
-
?
acetyl-CoA + heparan sulfate alpha-D-glucosaminide
CoA + heparan sulfate N-acetyl-alpha-D-glucosaminide
-
brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed
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?
?
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enzyme deficiency leads to Sanfilippo syndrome type C, i.e. mucopolysaccharidosis III C
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?
additional information
?
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enzyme deficiency leads to Sanfilippo syndrome type C, i.e. mucopolysaccharidosis III C
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?
additional information
?
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enzyme deficiency leads to Sanfilippo syndrome type C, i.e. mucopolysaccharidosis III C
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?
additional information
?
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enzyme deficiency causes mucopolysaccharidosis type IIIC
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?
additional information
?
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enzyme is acetylated at the cytoplasmic side of the lysosome and the acetyl group is then transferred to the inside where it is used to acetylate heparan sulfate
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?
additional information
?
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enzyme is acetylated at the cytoplasmic side of the lysosome and the acetyl group is then transferred to the inside where it is used to acetylate heparan sulfate
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-
?