Recent advances in ab initio direct methods have enabled the solution of cr
ystal structures of small proteins from native X-ray data alone, that is, w
ithout the use of fragments of known structure or the need to prepare heavy
-atom or selenomethionine derivatives, provided that the data are available
to atomic resolution. These methods are also proving to be useful for loca
ting the selenium atoms or other anomalous scatterers in the multiple wavel
ength anomalous diffraction phasing of larger proteins at lower resolution.