-
humans is
encoded by the
HADHB gene.
HADHB is a
subunit of the
mitochondrial trifunctional protein and has
thiolase activity. The
HADHB gene is
located on chromosome...
- ATP6AP2. The
level of
renin mRNA
appears to be
modulated by the
binding of
HADHB, HuR and CP1 to a
regulatory region in the 3' UTR. The gene for renin, REN...
- thiolase/enoyl-Coenzyme A
hydratase (trifunctional protein),
alpha subunit HADHB: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme...
- is a hetero-octamer
composed of four
alpha and four beta subunits:
HADHA HADHB The
three functions are 2-enoyl
coenzyme A (CoA) hydratase, long-chain 3-hydroxy...
-
trifunctional protein deficiency is
based on
mutations in the
HADHA and
HADHB genes which cause this disorder.
These genes each
provide instructions for...
- 3-Ketoacyl-CoA thiolase; β-Ketothiolase 3-KAT ACAA1
peroxisomal ACAA2
mitochondrial HADHB mitochondrial EC 2.3.1.154 Propionyl-CoA C2-trimethyltridecanoyltransferase...
- HGNC:17856 Q9UJ83 6893 HADH HGNC:4799 Q16836 6894
HADHA HGNC:4801 P40939 6895
HADHB HGNC:4803 P55084 6896 HAGH HGNC:4805 Q16775 6897
HAGHL HGNC:14177 Q6PII5...
- present. The
alpha subunit catalyzes this reaction, and is
attached to
HADHB,
which catalyzes the last step of the reaction.
Mutations in this gene result...
-
Beveridge DJ, van der
Weyden L,
Mangs H,
Leedman PJ,
Morris BJ (2003). "
HADHB, HuR, and CP1 bind to the
distal 3'-untranslated
region of
human renin mRNA...
- FASTKD2;
Fatty acid beta
oxidation pathway proteins (ACADVL, ECHS1, HADHA,
HADHB, ACAA2);
Amino acid
catabolic pathways proteins (MCCC1, MCCC2, GLUD1, HIBADH...
