ⓘ 4-Hydroxyphenylpyruvate dioxygenase

                                     

ⓘ 4-Hydroxyphenylpyruvate dioxygenase

4-Hydroxyphenylpyruvate dioxygenase, also known as α-ketoisocaproate dioxygenase, is an Fe-containing non-heme oxygenase that catalyzes the second reaction in the catabolism of tyrosine - the conversion of 4-hydroxyphenylpyruvate into homogentisate. HPPD also catalyzes the conversion of phenylpyruvate to 2-hydroxyphenylacetate and the conversion of α-ketoisocaproate to β-hydroxy β-methylbutyrate. HPPD is an enzyme that is found in nearly all aerobic forms of life.

                                     
  • 4 - Hydroxyphenylpyruvate dioxygenase HPPD inhibitors HPPD inhbitors are a class of herbicides that prevent plants by blocking 4 - Hydroxyphenylpyruvate
  • tyrosine involves the conversion of 4 - hydroxyphenylpyruvate to homogentisate by 4 - Hydroxyphenylpyruvate dioxygenase Complete deficiency of this enzyme
  • enzyme class is 4 - hydroxyphenylpyruvate oxygen oxidoreductase decarboxylating This enzyme is also called 4 - hydroxyphenylpyruvate dioxygenase II. Choroba
  • intermediary compound in the biosynthesis of scytonemin. 4 - Hydroxyphenylpyruvate dioxygenase Brand, Larry Harper, Alfred 1974 Effect of glucagon
  • 4 - Hydroxyphenylpyruvate oxygen oxidoreductase may refer to: 4 - hydroxyphenylpyruvate dioxygenase 4 - hydroxymandelate synthase
  • is a rare disorder caused by a deficiency of the enzyme 4 - hydroxyphenylpyruvate dioxygenase EC 1.13.11.27 encoded by the gene HPD. This enzyme is
  • inhibitors, which all work by inhibiting the plant enzyme 4 - hydroxyphenylpyruvate dioxygenase In plants, HPPD is necessary for carotenoid biosynthesis
  • action of nitisinone involves reversibile inhibition of 4 - Hydroxyphenylpyruvate dioxygenase HPPD This is a treatment for patients with Tyrosinemia
  • to incorporate an NIH shift in their mechanism, including 4 - hydroxyphenylpyruvate dioxygenase and the tetrahydrobiopterin dependent hydroxylases. The name
  • from a mutation in the HPD gene, which encodes the enzyme 4 - hydroxyphenylpyruvate dioxygenase Type III tyrosinemia is the rarest of the three conditions
  • to produce 4 - hydroxyphenylpyruvate 4 - Hydroxyphenylpyruvate is then oxidized by 4 - hydroxymandelate synthase 4 HmaS using oxygen to form 4 - hydroxymandelate