Hi Tim,

I only tried HKL2000, and index with different resolution and different
number of images. I am not quite familiar with XDS or d*trek.

One thing I am not sure is if this large oscillation angle will cause
problem in indexing?
If this is true, any method to overcome it?

The situation I met was when I chose different settings to do index,
HKL2000 would give different cell dimensions while most of them were not
small enough for a peptide crystal. The unit cell should be pretty small
since even collecting data with 5 degree oscillation angle, the spots in
one image were still fewer than a normal protein crystal case, so there is
no spots overlap.

Best,
Yang

On Thu, Mar 14, 2013 at 5:20 AM, Tim Gruene <t...@shelx.uni-ac.gwdg.de> wrote:

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> Dear Niu,
>
> could you let us know more about what you have already tried?
>
> - - use more images, maybe all images for indexing
> - - try a different program: xds instead of mosflm instead of hkl200
> instead of d*trek instead of xds .... depending what you have tried.
> - - try to find the unit cell dimensions manually from adxv
> - - try cell_now with the SPOTS.XDS
>
> in XDS I would check the output of IDXREF.LP to figure out if indexing
> seems possible, i.e. if the input parameters seem stable or if they
> are just floating around
>
> and many more - it depends on the data set, really!
>
> Best,
> Tim
>
> On 03/13/2013 09:12 PM, Niu Tou wrote:
> > Dear colleagues,
> >
> > We have some diffraction data from small peptide crystals, the
> > shape of diffraction spots looks normal, and resolution is beyond
> > 2A. The data were collected with 5 degree rotation per image. Later
> > on we found it is hard to do index. Does anybody know some skills
> > to figure this problem?
> >
> > Best wishes, Niu
> >
>
> - --
> - --
> Dr Tim Gruene
> Institut fuer anorganische Chemie
> Tammannstr. 4
> D-37077 Goettingen
>
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