| Information | |
|---|---|
| has gloss | eng: 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 |
| lexicalization | eng: tyrosine aminotransferase |
| instance of | (noun) any of various enzymes that move a chemical group from one compound to another compound transferase |
| Meaning | |
|---|---|
| Castilian | |
| has gloss | spa: 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. |
| lexicalization | spa: tirosina transaminasa |
| Media | |
|---|---|
| media:img | 3strucfinal.jpg |
| media:img | DimerTAT.jpg |
| media:img | Lys280plp.jpg |
| media:img | Pancakejpeg.jpg |
| media:img | ReactionTAT.jpg |
| media:img | TATActivesite.jpg |
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