EC Number   |
Inhibitors |
Structure |
|---|
    4.2.1.113 | EDTA |
loses all activity during treatment with EDTA, activity is most efficiently restored by Mn2+ |
   |
| 4.2.1.113 | more |
docking of potential inhibitors, inhibitor development via competitive binding of the substrate, overview. Design of a substrate-based analogue, evaluation of auxiliary molecule interaction energies through molecular docking and molecular dynamic simulation studies |
|
| 4.2.1.113 | more |
ligand docking interactions analysis, potential of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate substrate (SHCHC) derivatives as competitive enzyme inhibitors, overview |
|
| 4.2.1.113 | N-succinylphenylglycine |
competitive inhibition, molecular modeling showing that AaOSBS binds N-succinylphenylglycine with moderate affinity in a site that overlaps its normal substrate |
|
