Combining Evolutionary Conservation and Quantum Topological Analyses To Determine Quantum Mechanics Subsystems for Biomolecular Quantum Mechanics/Molecular Mechanics Simulations

Selection of residues and other molecular fragments for inclusion in the quantum mechanics (QM) region for QM/ molecular mechanics (MM) simulations is an important step for these calculations. Here, we present an approach that combines protein sequence/structure evolution and electron localization function (ELF) analyses. The combination of these two analyses allows the determination of whether a residue needs to be included in the QM subsystem or can be represented by the MM environment. We have applied this approach on two systems previously investigated by QM/MM simulations, 4-oxalocrotonate tautomerase (4OT) and ten-eleven translocation-2 (TET2), that provide examples where fragments may or may not need to be included in the QM subsystem. Subsequently, we present the use of this approach to determine the appropriate QM subsystem to calculate the minimum energy path (MEP) for the reaction catalyzed by human DNA polymerase lambda (Pol lambda) with a third cation in the active site. Our results suggest that the combination of protein evolutionary and ELF analyses provides insights into residue/ molecular fragment selection for QM/MM simulations.

Automated summary

This study presents an approach that combines protein sequence/structure evolution and electron localization function (ELF) analyses to determine which residues need to be included in the quantum mechanics (QM) region for QM/molecular mechanics (MM) simulations. The results suggest that this combination provides insights into residue/molecular fragment selection for QM/MM simulations.