Transamination

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Transamination (or aminotransfer) is the reaction between an amino acid and an alpha-keto acid. The amino group is transferred from the former to the latter; this results in the amino acid being converted to the corresponding α-keto acid, while the reactant α-keto acid is converted to the corresponding amino acid (if the amino group is removed from an amino acid, an α-keto acid is left behind).

Transamination in biochemistry is accomplished by enzymes called transaminases or aminotransferases. The human body synthesizes the 10 non-essential amino acids and transamination is the process by which most of these syntheses occur. The chirality of an amino acid is determined during transamination. This reaction uses the coenzyme PLP, and is considered to be a kinetically perfect reaction. The product of transamination reactions depend on the availability of alpha-keto acids. The products usually are either alanine, aspartate or glutamate, since their corresponding alpha-keto acids are produced through metabolism of fuels.

See also

• Transaminase

External links

• Overview of amino acid synthesis
• The chemical logic behind aminoacid degradation and the urea cyclecs:Transaminace

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