EC Number |
Title |
Organism |
---|
5.3.2.6 | Demethionylation of Pro-1 variants of 4-oxalocrotonate tautomerase in Escherichia coli by co-expression with an engineered methionine aminopeptidase |
Pseudomonas putida |
5.3.2.6 | Evidence for the formation of an enamine species during aldol and Michael-type addition reactions promiscuously catalyzed by 4-oxalocrotonate tautomerase |
Pseudomonas putida |
5.3.2.6 | Identification and characterization of new family members in the tautomerase superfamily analysis and implications |
Pseudomonas putida |
5.3.2.6 | Immobilization of Escherichia coli cells expressing 4-oxalocrotonate tautomerase for improved biotransformation of beta-nitrostyrene |
Pseudomonas putida |
5.3.2.6 | Importance of N-terminal proline for the promiscuous activity of 4-oxalocrotonate tautomerase (4-OT) |
Pseudomonas putida |
5.3.2.6 | Inactivation of 4-oxalocrotonate tautomerase by 5-halo-2-hydroxy-2,4-pentadienoates |
Leptothrix cholodnii |
5.3.2.6 | Inactivation of 4-oxalocrotonate tautomerase by 5-halo-2-hydroxy-2,4-pentadienoates |
Pseudomonas putida |
5.3.2.6 | Inactivation of 4-oxalocrotonate tautomerase by 5-halo-2-hydroxy-2,4-pentadienoates |
Leptothrix cholodnii SP-6 |
5.3.2.6 | Synthesis of gamma-nitroaldehydes containing quaternary carbon in the alpha-position using a 4-oxalocrotonate tautomerase whole-cell biocatalyst |
Pseudomonas putida |
5.3.2.6 | The S. aureus 4-oxalocrotonate tautomerase SAR1376 enhances immune responses when fused to several antigens |
Staphylococcus aureus |