[ccp4bb]: Re-indexing

[Jack Tanner <tannerjj@missouri.edu>]

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We ran into a similar reindexing problem in P21 that occurred after soaking
native crystals with an inhibitor.  It turned out to be the diagonal
construction that Clemens pointed out.  For details, see the Materials and
Methods section of


Tanner, J. J., Tu, S.-C., Barbour, L. J., Barnes, C. L. & Krause, K. L.
(1999) Unusual Folded Conformation of NAD+ Bound to Flavin Reductase P.
Protein Science,8, 1725-1732,

which can be found at

http://chem.chem.missouri.edu/TannerGroup/people/tanner/tannercv.html







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>
>Hi
>We recently re-collected a higher resolution data set on a crystal
>The new cell is 111 88 110 beta = 98 vs
>110 88 145 beta 131.5 for the old cell
>
>Both cells are P21
>
>The cells have appoximately the same volume. I have seen this type of
>choice of cell during indexing before and suspect both cells are the same.
>
>However, straight scaling of the data to each other goes haywire, so does
>transposing hkl to lkh.
>
>Anyone know how to do this. I don't fancy going back to tape and trying
>to force processing in the 'old' cell.
>best
>Jim
>
>James H. Naismith                | Research mailto:naismith@st-and.ac.uk
>Centre for Biomolecular Sciences | Teaching mailto:jhn@st-and.ac.uk
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Dr. John J. Tanner
Department of Chemistry
University of Missouri - Columbia
125 Chemistry Building
Columbia, MO 65211
USA

office: 573-884-1280
lab:    573-884-1281
fax:    573-882-2754
tannerjj@missouri.edu
http://www.chem.missouri.edu/TannerGroup/tanner.html
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