- 4-hydroxyphenylpyruvate
dioxygenase to
yield homogentisate. If
active and present, the
enzyme homogentisate 1,2-dioxygenase
further degrades homogentisic...
-
Homogentisate 1,2-dioxygenase (homogentisic acid oxidase,
homogentisate oxidase, homogentisicase) is an
enzyme which catalyzes the
conversion of homogentisate...
-
disease which is
caused by a
mutation in the HGD gene for the
enzyme homogentisate 1,2-dioxygenase (EC 1.13.11.5); if a
person inherits an
abnormal copy...
- off CO2
homogentisate (2,5-dihydroxyphenyl-1-acetate). In
order to
split the
aromatic ring of
homogentisate, a
further dioxygenase,
homogentisate 1,2-dioxygenase...
- autosomal-recessive disease,
known as alkaptonuria, that is
caused by a lack of
homogentisate oxidase enzyme.
Exogenous ochronosis is an
avoidable dermatitis that...
-
catabolism of
tyrosine - the
conversion of 4-hydroxyphenylpyruvate into
homogentisate. HPPD also
catalyzes the
conversion of
phenylpyruvate to 2-hydroxyphenylacetate...
-
solanesyl diphosphate is
synthesized through the MEP/DOXP pathway.
Homogentisate is
formed from p-hydroxyphenylpyruvate and is then
combined with solanesyl...
-
dietary components or drugs,
porphyrins in
patients with porphyria, and
homogentisate in
patients with alkaptonuria. Bile
pigment Bilirubin Biliverdin Heme...
-
inborn error of
metabolism caused by
mutations in the HGO gene and
homogentisate 1,2-dioxygenase deficiency.
Pseudoxanthoma elasti**** - rare multisystem...
- acid
tyrosine involves the
conversion of 4-hydroxyphenylpyruvate to
homogentisate by 4-hydroxyphenylpyruvate dioxygenase.
Complete deficiency of this...
