Β-N-acetylhexosaminidase
Term · Chemistry · MLC-T-CHM-001401
A lysosomal enzyme that catalyzes the hydrolysis of terminal N-acetyl-D-hexosamines from glycoconjugates. This enzyme exists as two major isoenzymes, Hex A and Hex B, which differ in their subunit composition. Deficiencies in this enzyme, particularly Hex A, lead to the accumulation of gangliosides, causing lysosomal storage disorders like Tay-Sachs disease.
| Identifier | MLC-T-CHM-001401 |
|---|---|
| Field | Chemistry |
| Subject | Chemistry and Human Health |
| Synonyms | hexosaminidase A |
| References | PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 715 (https://doi.org/10.1515/pac-2015-1202) |
| See also | Tay-Sachs disease |
Record as JSON
{
"id": "MLC-T-CHM-001401",
"term": "Β-N-acetylhexosaminidase",
"field": "Chemistry",
"definition": "A lysosomal enzyme that catalyzes the hydrolysis of terminal N-acetyl-D-hexosamines from glycoconjugates. This enzyme exists as two major isoenzymes, Hex A and Hex B, which differ in their subunit composition. Deficiencies in this enzyme, particularly Hex A, lead to the accumulation of gangliosides, causing lysosomal storage disorders like Tay-Sachs disease.",
"synonyms": [
"hexosaminidase A"
],
"subject": "Chemistry and Human Health",
"see_also": [
"Tay-Sachs disease"
],
"references": [
"PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 715 (https://doi.org/10.1515/pac-2015-1202)"
],
"url": "https://mlchart.com/terminology/chemistry/b-n-acetylhexosaminidase/"
}
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