First of all, thanks very much for those who replied to my question.
For those who do not follow this thread, I was asking a cryo question about
membrane protein crystals grown at 4C with 0.05-0.2M AS (ammonium sulfate) and
15-26%PEG400.
Some of you suggested directly freeze the crystal in LN
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I'm sure many of you have been in this situation before, so I would
be interested in your opinion.
I'm about to submit a paper containing the structure of a liganded
protein. The ligand itself is rather uninteresting, but it induces an
important conformational change. I solved a second
shivesh kumar wrote:
Dear all,
Can u suggest me any method to detwin the twinning data(2.2A).Any
suggestions are welcome.Thanx in advance.
Shivesh
Hi Shivesh,
For a partially twinned dataset with a twinning fraction not too close
to 0.5, from the command line:
% mkdir my_dir
% sfcheck
