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tyrosine aminotransferase (L-tyrosine:2-oxoglutarate aminotransferase, TAT)

Function: - catalyzes the 1st step in the catabolism of tyrosine, the reversible transfer of the amino group of tyrosine to 2-oxo-glutarate to form 4-hydroxyphenylpyruvate & L-glutamate - amino-acid degradation; L-phenylalanine degradation - acetoacetate & fumarate from L-phenylalanine: step 2/6 L-tyrosine + 2-oxoglutarate 4-hydroxyphenylpyruvate + L-glutamate Cofactor: pyridoxal phosphate (putative) Structure: - homodimer (putative) - belongs to the class-1 pyridoxal-phosphate-dependent aminotransferase family Pathology: - defects in TAT are the cause of tyrosinemia type 2

Related

TAT gene mutation tyrosine aminotransferase gene tyrosinemia type 2 (Richner-Hanhart syndrome)

General

aminotransferase

Properties

SIZE: entity length = 454 aa MW = 50 kD MOTIF: cofactor-binding site [280-280] FOR-BINDING-OF: pyridoxal phosphate

Database Correlations

OMIM 276600 UniProt P17735 PFAM correlations KEGG correlations ENZYME 2.6.1.5

References

  1. Stedman's Medical Dictionary 27th ed, Williams & Wilkins, Baltimore, 1999
  2. UniProt :accession P17735
  3. GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=TAT