EC Number |
Reaction |
Reference |
---|
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
- |
- |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
a catalytic triad is formed by residues Ser221, Glu353, and His466 |
651131 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
a catalytic triad is formed by residues Ser224, Glu341, and His452 |
651131 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
a catalytic triad is formed by residues Ser227, Glu344, and His456 |
651131 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
a catalytic triad is formed by residues Ser230, Glu347, and His459 |
651131 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
active site residues are Ser203, His448, and Asp97 |
-, 650852 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
active site structure, catalytic triad consists of residues Ser82, His235, and Asp207 |
652416 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
active site structure, substrate binding and reaction mechanism |
652562 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
catalytic mechanism for hydrolysis occurring at the methyl ester group in CE-1-cocaine, quantum mechanical/molecular mechanical (QM/MM) reaction-coordinate calculations, overview |
751606 |
3.1.1.1 | a carboxylic ester + H2O = an alcohol + a carboxylate |
catalytic triad consists of S162, H290, and D260 and is located at the bottom of a solvent accessible pocket. The guanidine moiety close to H290 confers a low pH shift of the catalytic His molecule |
668463 |