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Literature summary extracted from
- Stereospecificity of phenylpyruvate tautomerase. A convenient method for the preparation of chirally labelled phenylpyruvates (1977), Eur. J. Biochem., 72, 251-257.
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 5.3.2.1 | Bos taurus | - |
- |
- |
Source Tissue
| EC Number | Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|---|
| 5.3.2.1 | kidney | - |
Bos taurus | - |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 5.3.2.1 | 3-(4-hydroxyphenyl)pyruvate | keto-form | Bos taurus | 2-hydroxy-3-(4-hydroxyphenyl)prop-2-enoate | - |
? |  |
| 5.3.2.1 | Phenylpyruvate | r | Bos taurus | Phenylpyruvate | enol-form | ? | |
| 5.3.2.1 | 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 | ? | |
| 5.3.2.1 | Phenylpyruvate | keto-form | Bos taurus | Phenylpyruvate | enol-form | ? | |
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Release 2023.1 (January 2023)
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