Stephen,
Stephen,
Although your peptide is smaller than the one I once worked on, here are some
thoughts that might be applicable.
1. Check and play with the radius of integration in the molecular replacement.
The default is probably not appropriate for your case but the value should be
much
Hi All,
Just wanted to update this field in case someone in the future runs into the
same problem as me. The problem was concerning the Laminex plates with the
thick UV lid. The thickness of the lid cannot be stressed enough. While very
good for preventing evaporation it was simply not practic
University of Texas Medical Branch
3 Senior Faculty in Cryo Electron Microscopy, X-ray Crystallography, and
NMR
Sealy Center for Structural Biology & Molecular Biophysics
UTMB Health seeks senior faculty applicants in structural biolo
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Funded Access to Automated Crystallization Screening and in plate x-ray
analysis
a
Dear Stephen,
I guess you checked the processing that your huge unit cell is real. Did you
try epmr? In this case an evolutionary search may be the most suitable method,
but it could take a huge amount of cpu time.
Some comments:
Having about 40 monomers in the asymmetric unit could well explai
