EC Number   |
Reaction |
Reference |
|---|
   3.1.1.11 | pectin + n H2O = n methanol + pectate |
- |
- |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
mechanism |
651294, 652128 |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
reaction mechanism |
678803, 682960 |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
reaction mechanism, D157, stabilized by a hydrogen bond to R225, performs a nucleophilic attack on the ester bond of the carboxymethyl group of HGA |
682960 |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
reaction mechanism, the active site contains two aspartic acid residues D136 and D157 at the centre, which are distinguishing features of aspartyl esterases, two glutamines Q113 and Q135 and one arginine residue R225 |
682960 |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
the catalytic residues Gln151, Gln173, Asp174, Asp195, and Arg253 are conserved in Sal k 1 |
679294 |
| 3.1.1.11 | pectin + n H2O = n methanol + pectate |
two conserved aspartates are the nucleophile and general acid-base in the reaction mechanism, respectively, the catalytic site is formed by the conserved resisues Asp178, Asp199, and Arg267, molecular basis of the processive action of the enzyme, overview |
679502 |
