e/Tyrosine aminotransferase

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Information
has glosseng: 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. Mechanism
lexicalizationeng: tyrosine aminotransferase
instance of(noun) any of various enzymes that move a chemical group from one compound to another compound
transferase
Meaning
Castilian
has glossspa: La tirosina transaminasa o TyrAT (EC ) es una enzima que cataliza la reacción de transferencia de un grupo amino desde la L-tirosina al 2-oxoglutarato formándose L-glutamato y 4-hidroxifenilpiruvato. Esta enzima utiliza el piridoxal 5'-fosfato como cofactor.
lexicalizationspa: tirosina transaminasa
Media
media:img3strucfinal.jpg
media:imgDimerTAT.jpg
media:imgLys280plp.jpg
media:imgPancakejpeg.jpg
media:imgReactionTAT.jpg
media:imgTATActivesite.jpg

Query

Word: (case sensitive)
Language: (ISO 639-3 code, e.g. "eng" for English)


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