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Figure 1
A flow chart describing the sequence of events undertaken in this study. Purified protein was received and initial screening via sitting-drop vapor-diffusion experiments was set up. If initial crystals were single and harvestable, they were analyzed via X-ray diffraction. If the initial protein crystals produced high-quality X-ray diffraction data, the structure was solved without MPCS optimization. However, if the initial X-ray diffraction data were poor, or if the initial crystals were small or not harvestable, the crystals were optimized using the MPCS.

Journal logoJOURNAL OF
APPLIED
CRYSTALLOGRAPHY
ISSN: 1600-5767
Volume 43| Part 5| October 2010| Pages 1078-1083
https://doi.org/10.1107/S0021889810027378
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