-
reverse (cleaving an aldol), such as
Sialic acid
aldolase,
which forms sialic acid. See the list of
aldolases.
class I
proteins form a
protonated Schiff base...
-
Gamblin SJ,
Davies GJ,
Grimes JM (1991). "Activity and
specificity of
human aldolases".
Journal of
Molecular Biology. 219 (4): 573–576. doi:10.1016/0022-2836(91)90650-U...
- Unqualified,
aldolase usually refers to the
enzyme fructose-bisphosphate
aldolase.
Aldolase may also
refer to:
Aldolase A
Aldolase B
Aldolase C 17a-hydroxyprogesterone...
-
inborn error of
fructose metabolism caused by a
deficiency of the
enzyme aldolase B.
Individuals affected with HFI are
asymptomatic until they
ingest fructose...
-
dihydroxyacetone phosphate (DHAP), also a 3-carbon molecule.[citation needed]
Aldolase and fructose-1,6-bisphosphatase
convert a G3P and a DHAP into fructose...
- 1-phosphate.
Aldolase B
exhibits no
preference and thus
catalyzes both reactions,
while aldolases A and C
prefer FBP. In humans,
aldolase B is encoded...
- deoxyribose-5-phosphate
aldolase, 2-deoxyribose-5-phosphate
aldolase, and 2-deoxy-D-ribose-5-phosphate acetaldehyde-lyase.
Amongst aldolases, DERA is one of the...
-
located in the
center of the
homotetrameric αβ-barrel
structure of
these aldolases. However,
several structural details set
ALDOC apart. For instance, the...
-
Aldolase A
deficiency is an
autosomal recessive metabolic disorder resulting in a
deficiency of the
enzyme aldolase A; the
enzyme is
found predominantly...
- 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...
