-
Hexosaminidase (EC 3.2.1.52, β-acetylaminodeoxyhexosidase, N-acetyl-β-D-
hexosaminidase, N-acetyl-β-
hexosaminidase, N-acetyl
hexosaminidase, β-hexosaminidase...
- gene on
chromosome 15,
which codes a
subunit of the
hexosaminidase enzyme known as
hexosaminidase A. It is
inherited in an
autosomal recessive manner...
-
Hexosaminidase A (alpha polypeptide), also
known as HEXA, is an
enzyme that in
humans is
encoded by the HEXA gene,
located on the 15th chromosome. Hexosaminidase...
-
disorder caused by the
inherited deficiency to
create functional beta-
hexosaminidases A and B.
These catabolic enzymes are
needed to
degrade the neuronal...
- Beta-
hexosaminidase subunit beta is an
enzyme that in
humans is
encoded by the HEXB gene.
Hexosaminidase B is the beta
subunit of the
lysosomal enzyme...
- C.
perfringens encodes for
eight hexosaminidases that
break down
hexosamines in the mucus.
These hexosaminidases belong to four
glycoside hydrolase...
-
genetic disorders that
result from a
deficiency of the
enzyme beta-
hexosaminidase. This
enzyme catalyzes the
biodegradation of
fatty acid derivatives...
- same enzyme, beta-
hexosaminidase. AB
variant is
caused by a
failure in the gene that
makes an
enzyme cofactor for beta-
hexosaminidase,
called the GM2 activator...
-
substrate 4-nitrophenyl N-acetyl-β-D-glucosamine.
Dispersin B is a β-
hexosaminidase that
specifically hydrolyzes β-1,6-glycosidic
linkages of acetylglucosamine...
-
insufficiency is Tay–Sachs disease, in
which patients lack the
enzyme hexosaminidase. One
example of
enzyme deficiency is the most
common type of phenylketonuria...
