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The connectivity-based phasing method currently allows ab initio determination of phases for several hundred reflections. In the case of large macromolecular crystals, these reflections correspond to a very low resolution and the structural information deduced essentially consists of the molecular packing and an approximate molecular envelope. However, when the unit cell is relatively small, such a phasing procedure can produce phases such that secondary-structure elements can be identified in the corresponding maps. In the case of the pheromone Er-1, all three α-helices present are seen in the ab initio phased maps. In the case of protein G, not only the α-­helix but also some individual β-strands are distinguishable.

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