Computational design of an amidase by combining the best electrostatic features of two promiscuous hydrolases
Miquel À. Galmés, Alexander R. Nödling, Kaining He, Louis Y. P. Luk, Katarzyna Świderek, Vicent Moliner
Abstract
of the inserted aspartate and counteracting the anticipated catalytic effect. This prediction was experimentally confirmed with a 1.3-fold increase in activity. The good agreement between theoretical and experimental results, as well as the linear correlation between the electrostatic properties and the activation energy barriers, suggest that the presented computational-based investigation can transform in an enzyme engineering approach.
Topics & Concepts
Candida antarcticaAmidaseRational designElectrostaticsMolecular dynamicsChemistryEsteraseActive siteBacillus subtilisLipaseEnzymeComputational chemistryCombinatorial chemistryNanotechnologyMaterials scienceOrganic chemistryBiologyPhysical chemistryGeneticsBacteriaEnzyme Catalysis and ImmobilizationProtein Structure and DynamicsEnzyme Structure and Function