| Abstract: | We previously described a new conformational search method, termed low-mode search (LMOD), and discussed its utility for conformational searches performed on cycloalkanes and a cyclic penta-peptide. 1 In this report, we discuss a rigorous implementation of mode following (c-LMOD) for conformational searching, and we demonstrate that for a conformational search involving cycloheptadecane, this rigorous implementation is capable of finding all of the previously known structures. To the best of our knowledge, this is the first computational proof that mode following can be used for conformational searches conducted on a complex molecular system. We show, however, that, as expected, it is generally inefficient to perform a conformational search in this manner. Nonetheless, c-LMOD has been shown to be an excellent method for conducting conformational analyses involving conformational interconversions, where the location of saddle points is important. We also describe refinement to our original LMOD procedure (l-LMOD) and discuss its utility for a difficult conformational search problem, namely locating the global minimum energy conformation of C39H80. For this search, l-LMOD combined with limited torsional Monte Carlo movement was able to locate the lowest energy structures yet reported, and significantly outperformed a pure torsional Monte Carlo and a genetic algorithm-based search. Furthermore, we also demonstrate the utility of l-LMOD combined with random translation/rotation of a ligand for the extremely difficult problem of docking flexible ligands into flexible protein binding sites on a system that includes 9-deaza-guanine-based inhibitors docked into the flexible biding site of PNP. ©1999 John Wiley & Sons, Inc. J Comput Chem 20: 1671–1684, 1999 |
