Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9577997 | Chemical Physics Letters | 2005 | 4 Pages |
Abstract
A PM3 parameter set for iron has been developed, which is appropriate for the active site of iron sulfur proteins having a single iron atom by fitting DFT data obtained for a redox site analogue. These parameters are then tested on a set of such analogues involving a variety of ligands, and show good agreement with both DFT and experimental data for these species. The use of these parameters within a two level ONIOM treatment of the protein rubredoxin, yields accurate predictions of the effect of the enzyme on both Fe-S bond lengths and inner sphere reorganization energies.
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Authors
Mahesh Sundararajan, Jonathan P. McNamara, Ian H. Hillier, Hong Wang, Neil A. Burton,