Dear Ralf,
Thank you very much for your reply.
OK, I stop worrying about solvent mask handling.
Maybe my diffraction data have many problems (anisotropy, packing
disorder, etc.) rather than solvent mask...
Thanks again for all,
K. Yamashita
2010/12/8 Ralf W. Grosse-Kunstleve
Hi Keitaro,
By the way, in this situation, I'm wondering what the appropriate way
for bulk solvent correction is. How is the solvent mask calculated in phenix.refine? Is the protein region, which overlaps with symmetry mates, included in solvent mask with smaller occupancies?
No, we're not doing anything special. -- I think it would be quite tricky to do something that's theoretically better than what we have right now, and I wouldn't be surprised if it didn't make any significant difference for the end results, after all the work.
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