MeSH definition : A hexosaminidase specific for non-reducing N-acetyl-D-hexosamine residues in N-acetyl-beta-D-hexosaminides.
It acts on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES. Two specific mammalian
isoenzymes of beta-N-acetylhexoaminidase are referred to as HEXOSAMINIDASE A and HEXOSAMINIDASE
B. Deficiency of the type A isoenzyme causes TAY-SACHS DISEASE, while deficiency of
both A and B isozymes causes SANDHOFF DISEASE. The enzyme has also been used as a
tumor marker to distinguish between malignant and benign disease.;
MeSH synonym : beta n acetylhexosaminidase; beta-n-acetyl-hexosaminidase; beta-n-acetyl-d-hexosaminidase; beta hexosaminidase; beta n acetyl d hexosaminidase; n-acetyl-beta-d-hexosaminidase; n acetyl beta d hexosaminidase; beta n acetyl hexosaminidase; beta-n-acetylhexosaminidase; beta-hexosaminidase; beta N acetylhexosaminidases;
MeSH CAS label : beta-N-Acetyl-D-hexosaminide N-acetylhexosaminohydrolase;
Registry Number MeSH : EC 3.2.1.52;
MeSH annotation : do not confuse with ACETYLGLUCOSAMINIDASE; /defic: consider also TAY SACHS DISEASE
and SANDHOFF DISEASE;
A hexosaminidase specific for non-reducing N-acetyl-D-hexosamine residues in N-acetyl-beta-D-hexosaminides.
It acts on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES. Two specific mammalian
isoenzymes of beta-N-acetylhexoaminidase are referred to as HEXOSAMINIDASE A and HEXOSAMINIDASE
B. Deficiency of the type A isoenzyme causes TAY-SACHS DISEASE, while deficiency of
both A and B isozymes causes SANDHOFF DISEASE. The enzyme has also been used as a
tumor marker to distinguish between malignant and benign disease.