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Aspartoacylase is a
hydrolytic enzyme (EC 3.5.1.15, also
called aminoacylase II, ASPA and
other names) that in
humans is
encoded by the ASPA gene. ASPA...
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which is
responsible for the
production of the
enzyme aspartoacylase.
Decreased aspartoacylase activity prevents the
normal breakdown of N-acetylaspartate...
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Student Press ****ociation ASPA (car), a 1920s
Czech car ASPA (gene),
Aspartoacylase, on
human chromosome 17
Autonomous System Provider Authorizations in...
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recessive pattern. It is due to a
mutation in the ASPA gene that
encodes aspartoacylase, an
enzyme needed to
metabolize N-acetyl-L-aspartate (NAA). The mutation...
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protein p53 (Li-Fraumeni syndrome),
tumor suppressor gene (17p13.1) ASPA:
aspartoacylase (Canavan disease) (17p13.3) GLOD4:
glyoxalase domain containing 4 (17p13...
- Canavan's disease: Canavan's
disease is a
white matter disease due to
aspartoacylase deficiency. The
dentate nucleus is not
affected until late in disease...
- by
aging (cg25809905 in integrin,
alpha 2b (ITGA2B); cg02228185 in
aspartoacylase (ASPA) and cg17861230 in
phosphodiesterase 4C, cAMP
specific (PDE4C))...
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neurotransmitter in the
brain by
acting on
metabotropic glutamate receptors.
Aspartoacylase Canavan disease "N-acetylaspartate -
Compound Summary".
PubChem Compound...
- 3.5.1.14: N-acyl-aliphatic-L-amino acid
amidohydrolase EC 3.5.1.15:
aspartoacylase EC 3.5.1.16:
acetylornithine deacetylase EC 3.5.1.17: acyl-lysine deacylase...
- system, also
known as Canavan's disease, Van Bogaert-Bertrand type or
Aspartoacylase (AspA) deficiency, is a rare
autosomal recessive neurodegenerative disorder...
