Abstract
A new phase-extension procedure has been applied to isomorphous replacement data and shown to yield improved phases and maps compared with standard solvent flattening operating on a full set of centroid phases. In this procedure, a starting subset of core phases is selected based on the sharpness of the phase-probability curves. Phase extension using solvent flattening as the density-modification procedure is then carried out, gradually adding additional phases. In tests with known protein structures, the mean phase errors for the output expanded phase sets were reduced by 3-9° and the corresponding map correlation coefficients were increased by 0.05-0.18 relative to phase sets from standard solvent-flattening procedures. With SIR data, the lowest final mean phase errors were approximately 58° and the corresponding map correlation coefficients were in the range 0.53-0.68.
| Original language | English |
|---|---|
| Pages (from-to) | 1048-1051 |
| Number of pages | 4 |
| Journal | Acta Crystallographica Section D: Biological Crystallography |
| Volume | 57 |
| Issue number | 7 |
| DOIs | |
| State | Published - 2001 |
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