C. Giacovazzo et al., THE AB-INITIO CRYSTAL-STRUCTURE SOLUTION OF PROTEINS BY DIRECT-METHODS .3. THE PHASE EXTENSION PROCESS, Acta crystallographica. Section A, Foundations of crystallography, 51, 1995, pp. 177-188
In two preceding papers [Giacovazzo, Siliqi and Ralph (1994). Acta Cry
st. A50, 503-510; Giacovazzo, Siliqi and Spagna (1994). Acta Cryst. A5
0, 609-621], a direct-phasing process was described which proved to be
potentially able to solve ab initio crystal structures of proteins. T
he method uses the diffraction data of the native and of one isomorpho
us derivative. The main limitation of the approach was the small numbe
r of phased reflections rather than the quality of the assigned phases
. In this paper, it is shown that the phasing process can be extended
to about 40% of the measured reflections (up to the derivative resolut
ion) without reducing significantly the quality of the new phases. Of
the four test proteins examined, in one case it was possible to obtain
fully interpretable electron-density maps.