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BRENDA support

Literature summary for 5.3.2.1 extracted from

  • Retey, J.; Bartl, K.; Ripp, E.; Hull, W.E.
    Stereospecificity of phenylpyruvate tautomerase. A convenient method for the preparation of chirally labelled phenylpyruvates (1977), Eur. J. Biochem., 72, 251-257.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Bos taurus
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-
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Source Tissue

Source Tissue Comment Organism Textmining
kidney
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Bos taurus
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3-(4-hydroxyphenyl)pyruvate keto-form Bos taurus 2-hydroxy-3-(4-hydroxyphenyl)prop-2-enoate
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?
Phenylpyruvate r Bos taurus Phenylpyruvate enol-form ?
Phenylpyruvate converts the enol-form to the keto-form by incorporating a solvent proton into the pro-R position, in the reverse reaction the same pro-R proton is abstracted Bos taurus Phenylpyruvate enol-form ?
Phenylpyruvate keto-form Bos taurus Phenylpyruvate enol-form ?