Dear Manoj,

providing your crystals diffract to at least 2.5 Å and the sulfurs are
ordered, you should be able to solve your structure without too many
problems.  As a first experiment, I would recommend collecting 360 degrees
of data.  Process these with XDS and the FRIEDEL'S_LAW= FALSE option and
see how much anomalous signal CORRECT.LP reports, if you've got stars in
the values of the Anomal Corr column, you're on the right track.  Try to
phase with SHELXD, following the advice on http://shelx.uni-goettingen
.de/tutorials.php.

If you don't succeed, you might need higher multiplicity.  If you have a
kappa or chi goniometer, you can reorient the crystal and collect another
360 degrees and another 360 degrees, and so on.  Merge all data in XSCALE
until you can solve the structure.

I once wrote a little tutorial for doing S-SAD on the home source that you
might want to follow.  http://www.imperial.ac.uk/x-
ray-crystallography/learning-more/sulphur-sad/  With an HPC detector (or
even an image plate) you'd getter better data than with a CCD detector and
be able to solve your structure quicker.  (Disclaimer: I work for a company
that makes HPC detectors.)  I consider the home source a great place to
solve structures by native SAD.

All best.


Andreas



On Tue, Apr 3, 2018 at 4:26 PM, Manoj Saxena <00001d16aa30e8a1-dmarc-reques
t...@jiscmail.ac.uk> wrote:

> Hi All,
>
> I am writing to seek advice on doing  sulphur SAD data collection
> at Cu based home source for a protein that is 12 KDa and has 6 S atoms.
> I have seen some links online and some references but would be grateful if
> you can share your know-how for success with this.
> Like what multiplicity of data would be good to aim for and
> data processing tips.
> Inputs from people who have tried and failed would also be highly
> appreciated.
>
> Thank you
> Manoj Saxena
> University of Puerto Rico
>
>
>


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