Any feedback?
Literature summary for 4.1.1.4 extracted from
- The interactions of acetoacetate decarboxylase with carbonyl compounds, hydrogen cyanide, and an organic mercurial (1970), J. Biol. Chem., 245, 5214-5222.
Inhibitors
| Inhibitors | Comment | Organism | Structure |
|---|---|---|---|
| beta-Diketones | - |
Clostridium acetobutylicum | |
| Borohydride | - |
Clostridium acetobutylicum |  |
| HCN- | inhibitory synergism between cyanide and carbonyl compounds. The effectiveness in descending order: acetaldehyde, acetone, cyclohexanone, methyl ethyl ketone, 3-hexanone, diethyl ketone | Clostridium acetobutylicum | |
| p-chloromercuriphenyl sulfonate | reversal by Cys | Clostridium acetobutylicum | |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Clostridium acetobutylicum | - |
- |
- |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2-Oxo-3-phenylpropionic acid | i.e. phenylacetoacetate | Clostridium acetobutylicum | Acetophenone + CO2 | - |
? | |
| Acetoacetate | - |
Clostridium acetobutylicum | Acetone + CO2 | - |
? | |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
