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TAT

Function

Transaminase involved in tyrosine breakdown. Converts tyrosine to p-hydroxyphenylpyruvate. Can catalyze the reverse reaction, using glutamic acid, with 2-oxoglutarate as cosubstrate (in vitro). Has much lower affinity and transaminase activity towards phenylalanine.

Involvement in disease

Tyrosinemia 2

TYRSN2

An inborn error of metabolism characterized by elevations of tyrosine in the blood and urine, and oculocutaneous manifestations. Typical features include palmoplantar keratosis, painful corneal ulcers, and intellectual disability.

None

The disease is caused by variants affecting the gene represented in this entry.

Pathway

Amino-acid degradation; L-phenylalanine degradation; acetoacetate and fumarate from L-phenylalanine: step 2/6.

Sequence Similarities

Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family.

Alternative names

Tyrosine aminotransferase, TAT, L-tyrosine:2-oxoglutarate aminotransferase

swissprot:P17735 entrezGene:6898 omim:613018