EC Number | Crystallization (Comment) | Organism |
---|---|---|
4.1.1.7 | in complex with methyl benzoylphosphonate, hanging drop vapor diffusion method, using 100 mM Tris-HCl (pH 8.5), 150 mM CaCl2, 22% (v/v) PEG 400 | Pseudomonas putida |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
4.1.1.7 | benzoylphosphonate | the reaction of methyl benzoylphosphonate with BFDC results in the formation of a stable analogue (C2alpha-phosphonomandelyl thiamine diphosphate) of the covalent thiamine diphosphate-substrate adduct C2alpha-mandelyl thiamine diphosphate | Pseudomonas putida | |
4.1.1.7 | methyl benzoylphosphonate | competitive inhibitor | Pseudomonas putida |
EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
4.1.1.7 | 0.76 | - |
methyl benzoylphosphonate | - |
Pseudomonas putida |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
4.1.1.7 | Pseudomonas putida | P20906 | - |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.1.1.7 | benzaldehyde + acetaldehyde | - |
Pseudomonas putida | (S)-2-hydroxypropiophenone | - |
r | |
4.1.1.7 | benzaldehyde + benzaldehyde | - |
Pseudomonas putida | (R)-benzoin | - |
r | |
4.1.1.7 | methyl benzoylphosphonate | - |
Pseudomonas putida | ? | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
4.1.1.7 | BFDC | - |
Pseudomonas putida |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
4.1.1.7 | thiamine diphosphate | - |
Pseudomonas putida |
EC Number | Ki Value [mM] | Ki Value maximum [mM] | Inhibitor | Comment | Organism | Structure |
---|---|---|---|---|---|---|
4.1.1.7 | 0.38 | - |
methyl benzoylphosphonate | - |
Pseudomonas putida |