enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 4-Hydroxyphenylpyruvate dioxygenase - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxyphenylpyruvate...

    HPPD also catalyzes the conversion of phenylpyruvate to 2-hydroxyphenylacetate and the conversion of α-ketoisocaproate to β-hydroxy β-methylbutyrate. [2] [3] HPPD is an enzyme that is found in nearly all aerobic forms of life. [4] This reaction shows the conversion of 4-hydroxyphenylpyruvate into homogentisate by HPPD.

  3. 4-Hydroxyphenylpyruvate dioxygenase inhibitor - Wikipedia

    en.wikipedia.org/wiki/4-hydroxyphenylpyruvate...

    4-Hydroxyphenylpyruvate dioxygenase (HPPD) is an enzyme found in both plants and animals, which catalyzes the catabolism of the amino acid tyrosine. [4] Preventing the breakdown of tyrosine has three negative consequences: the excess of tyrosine stunts growth; the plant suffers oxidative damage due to lack of tocopherols (vitamin E); and ...

  4. Nitisinone - Wikipedia

    en.wikipedia.org/wiki/Nitisinone

    The mechanism of action of nitisinone involves inhibition of 4-Hydroxyphenylpyruvate dioxygenase (HPPD). [5] [6] This is a treatment for patients with Tyrosinemia type 1 as it prevents the formation of 4-Maleylacetoacetic acid and fumarylacetoacetic acid, which have the potential to be converted to succinyl acetone, a toxin that damages the liver and kidneys. [4]

  5. Tyrosinemia type III - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_III

    Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27), encoded by the gene HPD. [2] This enzyme is abundant in the liver, and smaller amounts are found in the kidneys. It is one of a series of enzymes needed to break down tyrosine.

  6. Tyrosinemia type I - Wikipedia

    en.wikipedia.org/wiki/Tyrosinemia_type_I

    It modifies the function of 4-hydrooxyphenylpyruvate dioxygenase by acting as a competitive inhibitor. 4-hydrooxyphenylpyruvate dioxygenase functions to convert 4-hydroxyphenylpyruvate to homogentisate as the second enzymatic reaction in the tyrosine catabolic pathway. This prevents the further catabolism of tyrosine. [5]

  7. Tyrosine aminotransferase - Wikipedia

    en.wikipedia.org/wiki/Tyrosine_aminotransferase

    6898 234724 Ensembl ENSG00000198650 ENSMUSG00000001670 UniProt P17735 Q8QZR1 RefSeq (mRNA) NM_000353 NM_146214 RefSeq (protein) NP_000344 NP_666326 Location (UCSC) Chr 16: 71.57 – 71.58 Mb Chr 8: 110.72 – 110.73 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Tyrosine aminotransferase (or tyrosine transaminase) is an enzyme present in the liver and catalyzes the conversion of ...

  8. Alpha-ketoglutarate-dependent hydroxylases - Wikipedia

    en.wikipedia.org/wiki/Alpha-ketoglutarate...

    The uncoordinated end of the superoxide ligand attacks the keto carbon, inducing release of CO 2 and forming an Fe(IV)-oxo intermediate. This Fe=O center then oxygenates the substrate by an oxygen rebound mechanism. [1] [2] Alternative mechanisms have failed to gain support. [23] Consensus catalytic mechanism of the αKG-dependent dioxygenase ...

  9. 4-hydroxymandelate synthase - Wikipedia

    en.wikipedia.org/wiki/4-hydroxymandelate_synthase

    In enzymology, a 4-hydroxymandelate synthase (EC 1.13.11.46) is an enzyme that catalyzes the chemical reaction. 4-hydroxyphenylpyruvate + O 2 4-hydroxymandelate + CO 2. Thus, the two substrates of this enzyme are 4-hydroxyphenylpyruvate and oxygen, whereas its two products are 4-hydroxymandelate and carbon dioxide.