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tyrosine aminotransferase - tradução para russo
MAMMALIAN PROTEIN FOUND IN HOMO SAPIENS
Tyrosine transaminase; EC 2.6.1.5; TAT (gene); L-tyrosine:2-oxoglutarate aminotransferase
tyrosine aminotransferase
медицина
тирозинаминотрансфераза
tyrosine hydroxylase
![Tyrosine hydroxylase catalyzes the rate limiting step in [[catecholamine]] biosynthesis](https://commons.wikimedia.org/wiki/Special:FilePath/Catecholamines biosynthesis.svg?width=200 "Tyrosine hydroxylase catalyzes the rate limiting step in [[catecholamine]] biosynthesis")
![substrate]] would enter from.](https://commons.wikimedia.org/wiki/Special:FilePath/Tyrosine hydroxylase from rat showing two of its domains.png?width=200 "substrate]] would enter from.")
медицина
тирозингидроксилаза
diiodotyrosine
CHEMICAL COMPOUND
3,5-diiodo-L-tyrosine; ATC code H03BX01; ATCvet code QH03BX01; 3,5-diiodotyrosine; 3,5-Diiodotyrosine
фармацевтический термин
дийодтирозин (предшественник тироксина)
Definição
Tyrosin
·noun A white crystalline nitrogenous substance present in small amount in the pancreas and spleen, and formed in large quantity from the decomposition of proteid matter by various means, - as by pancreatic digestion, by putrefaction as of cheese, by the action of boiling acids, ·etc. Chemically, it consists of oxyphenol and amidopropionic acid, and by decomposition yields oxybenzoic acid, or some other benzol derivative.
Wikipédia
Tyrosine aminotransferase
Tyrosine aminotransferase (or tyrosine transaminase) is an enzyme present in the liver and catalyzes the conversion of tyrosine to 4-hydroxyphenylpyruvate.
In humans, the tyrosine aminotransferase protein is encoded by the TAT gene. A deficiency of the enzyme in humans can result in what is known as type II tyrosinemia, wherein there is an abundance of tyrosine as a result of tyrosine failing to undergo an aminotransferase reaction to form 4-hydroxyphenylpyruvate.
