X-ray crystallography remains the most dominant method for solving atomic structures. However, for relatively large systems, the availability of only medium-to-low-resolution diffraction data often limits the determination of all-atom details. A new molecular dynamics flexible fitting (MDFF)-based approach, xMDFF, for determining structures from such low-resolution crystallographic data is reported. xMDFF employs a real-space refinement scheme that flexibly fits atomic models into an iteratively updating electron-density map. It addresses significant large-scale deformations of the initial model to fit the low-resolution density, as tested with synthetic low-resolution maps of d-ribose-binding protein. xMDFF has been successfully applied to re-refine six low-resolution protein structures of varying sizes that had already been submitted to the Protein Data Bank. Finally, via systematic refinement of a series of data from 3.6 to 7Å resolution, xMDFF refinements together with electro physiology experiments were used to validate the first all-atom structure of the voltage-sensing protein Ci-VSP.
|Original language||English (US)|
|Number of pages||12|
|Journal||Acta Crystallographica Section D: Biological Crystallography|
|State||Published - Aug 26 2014|
- molecular dynamics flexible fitting
ASJC Scopus subject areas
- Structural Biology