Hello everyone.
I'm a begginer in crystallography, especially in EP and I'm trying to solve a
structure by SAD. Right now I'm trying to solve the substructure on shelxD by
running hkl2map, but I'm finding hard to chose between solutions. So I'm
asking, what should by my solution criteria (CCall
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Dear Andre,
as a rule of thumb you should cut the resolution for shelxd in SAD where
the anomalous selfCC as reported by shelxc drops below 30%. The second
important figure is a correct solvent content for shelxe, but only
really if you do not use the
I've collected data from crystal soaked with brightly coloured ligands
which partition into the solvent channels. Although the crystal becomes
highly coloured (mopping up most of the colour from the drop) the
structures remained resolutely empty. I am intrigued by this observation
and wonder how mu
This is the second announcement of an X-ray protein crystallography
course in Oulu, Finland, from January, 30 till February 3, 2012.
Further details of the outline of the program are given on the
WWW-site, as listed below. The topic of the course focuses on data
collection, data processing, data t
Typically provided that the dye does not kill the crystal, there is no
effect on structure, at least nothing I ever saw. The effect is similar to
sizing column.
Artem
On Nov 10, 2011 10:44 PM, "adam andres" wrote:
>
>
> Hi crystallographers
>
> Has anyone actually collected data on a crystal that
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