Tyrosine Aminotransferase

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Details

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Tyrosine aminotransferase 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. Structures of the three main molecules involved in chemical reaction catalyzed by the tyrosine aminotransferase enzyme are shown below: the amino acid tyrosine, the prosthetic group pyridoxal phosphate, and the resulting product 4-hydroxyphenylpyruvate.

Weitere Informationen

  • Allgemeine Informationen
    • GTIN 09786130973353
    • Editor Lambert M. Surhone, Miriam T. Timpledon, Susan F. Marseken
    • Größe H220mm x B220mm
    • EAN 9786130973353
    • Format Fachbuch
    • Titel Tyrosine Aminotransferase
    • Herausgeber Betascript Publishing
    • Anzahl Seiten 140
    • Genre Biologie

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