-
Aldolase A (ALDOA, or ALDA), also
known as fructose-bisphosphate
aldolase, is an
enzyme that in
humans is
encoded by the
ALDOA gene on
chromosome 16....
- Fructose-bisphosphate
aldolase (EC 4.1.2.13),
often just
aldolase, is an
enzyme catalyzing a
reversible reaction that
splits the aldol,
fructose 1,6-bisphosphate...
-
Aldolase B also
known as fructose-bisphosphate
aldolase B or liver-type
aldolase is one of
three isoenzymes (A, B, and C) of the
class I
fructose 1,6-bisphosphate...
-
Aldolase C, fructose-bisphosphate (ALDOC, or ALDC), is an
enzyme that, in humans, is
encoded by the
ALDOC gene on
chromosome 17. This gene
encodes a member...
-
Aldolase A
deficiency is an
autosomal recessive metabolic disorder resulting in a
deficiency of the
enzyme aldolase A; the
enzyme is
found predominantly...
-
inborn error of
fructose metabolism caused by a
deficiency of the
enzyme aldolase B.
Individuals affected with HFI are
asymptomatic until they
ingest fructose...
- trans-o-Hydroxybenzylidenepyruvate hydratase-
aldolase (EC 4.1.2.45, 2′-hydroxybenzalpyruvate
aldolase, NsaE,
tHBPA hydratase-
aldolase) is an
enzyme with
systematic name...
-
dihydroxyacetone phosphate (DHAP), also a 3-carbon molecule.[citation needed]
Aldolase and fructose-1,6-bisphosphatase
convert a G3P and a DHAP into fructose...
- The
enzyme 2-dehydro-3-deoxy-phosphogluconate
aldolase (EC 4.1.2.14),
commonly known as KDPG
aldolase,
catalyzes the
chemical reaction 2-dehydro-3-deoxy-D-gluconate...
- They are Nε-trimethyllysine hydroxylase, 3-hydroxy-Nε-trimethyllysine
aldolase, 4-N-trimethylaminobutyraldehyde
dehydrogenase and γ-butyrobetaine hydroxylase...
