Abstract
Bond bundle analysis is used to investigate enzymatic catalysis in the ketosteroid isomerase (KSI) active site. We identify the unique bonding regions in five KSI systems, including those exposed to applied oriented electric fields and those with amino acid mutations, and calculate the precise redistribution of electron density that accompanies either enhancement or inhibition of KSI catalytic activity. In two examples—using direct inspection of bond bundle regional properties, and using correlations between those properties and reaction barrier height—we arrive at similar conclusions, that catalytic enhancement results from promoting electron density redistribution between bonds within the KSI-docked substrate molecule in a way that closely resembles our mechanistic understanding of the forward catalyzed reaction. The catalyzing charge redistribution between bond bundles is prevalent in KSI systems catalyzed via electric fields or via amino acid mutation, and are thus suggestive of a general catalytic role.
Supplementary materials
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Supplementary information
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• 3D depictions of some of the regions discussed in the manuscript
• Coordinates and energies of ab-initio calculations
• Atomic basin, bond bundle, and bond wedge tabulated integration values with many more
properties than are included in this manuscript
• Mmulti-variable bar charts of simplified regional property correlations
• Plots of fits of each region and property with reaction barrier energy
• Correlations among regional properties
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Source code for analysis used in manuscript
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Source code for the gradient bundle decomposition algorithm and for the post-processing statistical analysis and plotting presented in the manuscript.
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