EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
2.6.1.B16 | F84A | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | F84G | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | F84L | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | F84W | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | I258A | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | I258G | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | I258V | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | additional information | four mutants of the amine transaminase from Halomonas elongata are generated by an in silico-based design and recombinantly produced in Escherichia coli, purified, and applied to the amination of mono-substituted aromatic carbonyl-derivatives. While benzaldehyde derivatives are excellent substrates, only NO2-acetophenones are transformed into the (S)-amine with a high enantioselectivity. The different behaviour of wild-type and mutated transaminases is assessed by in silico substrate binding mode studies, overview | Halomonas elongata |
2.6.1.B16 | W56A | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | W56F | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | W56G | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | W56L | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | Y149A | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | Y149F | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
2.6.1.B16 | Y149G | site-directed mutagenesis, substrate specificity analysis | Halomonas elongata |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.6.1.B16 | Halomonas elongata | - |
- |
- |
EC Number | Specific Activity Minimum [µmol/min/mg] | Specific Activity Maximum [µmol/min/mg] | Comment | Organism |
---|---|---|---|---|
2.6.1.B16 | 0.06 | - |
recombinant mutant F84A, pH 8.0, 25°C | Halomonas elongata |
2.6.1.B16 | 0.43 | - |
recombinant mutant I258A, pH 8.0, 25°C | Halomonas elongata |
2.6.1.B16 | 0.5 | - |
recombinant mutant Y149F, pH 8.0, 25°C | Halomonas elongata |
2.6.1.B16 | 3.99 | - |
recombinant wild-type enzyme, pH 8.0, 25°C | Halomonas elongata |
2.6.1.B16 | 4.43 | - |
recombinant mutant W56G, pH 8.0, 25°C | Halomonas elongata |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.6.1.B16 | (S)-1-phenylethylamine + pyruvate | - |
Halomonas elongata | L-alanine + acetophenone | - |
r | |
2.6.1.B16 | 2-nitroacetophenone + L-alanine | - |
Halomonas elongata | 2-nitro-(S)-1-phenylethylamine + pyruvate | - |
r | |
2.6.1.B16 | 3-nitroacetophenone + L-alanine | - |
Halomonas elongata | 3-nitro-(S)-1-phenylethylamine + pyruvate | - |
r | |
2.6.1.B16 | 4-nitroacetophenone + L-alanine | - |
Halomonas elongata | 4-nitro-(S)-1-phenylethylamine + pyruvate | - |
r | |
2.6.1.B16 | additional information | substrate specificity of wild-type and mutant enzymes, overview. No activity of mutant F84G with (S)-1-phenylethylamine. Analysis of activity of the enzymes with ortho-, meta-, and para-substituted derivatives of fluoroacetophenone, trifluoroacetophenone, methoxyacetophenone, methylacetophenone, nitrobenzaldehyde, fluorobenzaldehyde, trifluorobenzaldehyde, methoxybenzaldehyde, methylbenzaldehyde, and of benzaldehyde, docking study | Halomonas elongata | ? | - |
- |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
2.6.1.B16 | 25 | - |
assay at | Halomonas elongata |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
2.6.1.B16 | 8 | - |
assay at | Halomonas elongata |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
2.6.1.B16 | pyridoxal 5'-phosphate | - |
Halomonas elongata |
EC Number | General Information | Comment | Organism |
---|---|---|---|
2.6.1.B16 | additional information | four mutants of the amine transaminase from Halomonas elongata are generated by an in silico-based design and recombinantly produced in Escherichia coli, purified, and applied to the amination of mono-substituted aromatic carbonyl-derivatives. While benzaldehyde derivatives are excellent substrates, only NO2-acetophenones are transformed into the (S)-amine with a high enantioselectivity. The different behaviour of wild-type and mutated transaminases is assessed by in silico substrate binding mode studies, overview | Halomonas elongata |