| Abstract: | A computer algorithm is developed for integrating density functional quantum mechanics into a molecular mechanics program. The computationally infeasible aspects of the standard LCAO-MO approach (the iterative calculation of eigenvectors and the requirement of orthogonal expansions for the orbitals) are replaced with an efficient use of optimization via the trace theorem of linear algebra. The construction of a basis is also described for expanding the electron density that transforms with the molecular geometry. The combination of the trace method and the basis allow the solution for one configuration of atoms and electrons to be tracked over a wide range of internal conformations. The approach is readily adaptable to being used in the context of an imposed classical field that allows it to be used on part of a macromolecular complex. The initial implementation in the program AMMP is described. ©1999 John Wiley & Sons, Inc. J Comput Chem 20: 1618–1633, 1999 |
