th). I'm happy to answer informal enquiries at
j.irv...@ucl.ac.uk.
Best wishes,
James
Dr. James Irving
UCL Respiratory / Institute of Structural and Molecular Biology
University College London
London UK
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Hi Francis,
Detwinning of perfectly twinned data is done with reference to Fcalc
(determined from from the model): it is not possible to arithmetically
deconvolute the contribution of the twin domains to the perfectly twinned
reflection data.
Because your model is incomplete you will be introduci
pinions and suggestions!
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Dr. James Irving
NH&MRC C.J. Martin Fellow
School of Biomedical Science
You can check whether something strange is happening to your environment
variables within the PERL process by typing:perl -e 'print
join("\n",%ENV)."\n"' | more
hth
You can perform a multiple structural alignment using MUSTANG (
http://www.bx.psu.edu/arun/research/mustang/), which draws upon some of the
underpinnings of the DALI approach.
James
Hi Siva,
SFCHECK (part of CCP4i) has a very handy option for this. From the
command line:
% mkdir mydir
% sfcheck -f mydata.mtz -po mydir/ -out u -r
% gv mydir/sfcheck_.ps
(or ghostscript/xpsview/whatever postscript viewer you have)
This will generate a number of output files, includin
Hi Fred,
From memory, this can occur due to long bond lengths in the model being
interpreted as chain breaks, try editing the generate.inp or
generate_easy.inp script and increase the value for "break_cutoff":
{* cutoff distance in Angstroms for identification of breaks *}
{* the default of 2
I guess the point is to "know thy data", to avoid problems down the
track: a statistical test for twinning forms one of a battery of tests
which can be performed independently of a coordinate set (Matthews
coefficient, self-RF, etc.), and with relative ease. Importantly, in
the case of partial
th a partial twin fraction
close to 0.5 or perfectly twinned should not be detwinned, use SHELX or
CNS to refine against the twinned data instead.
HTH,
James
--
Dr. James Irving
NH&MRC C.J. Martin Fellow
Division of Structural Biology
Wellcome Trust Centre for Human Genetics
Oxford University
R
db' file). I get the error:
'Fatal error: wrong format in PDB file.'
..and the values in the B-factor (%Equivalent) column are all either 99 or
100 which is nonsense according to the alignment.
Has anyone come across this. I don't see anything wrong with my PDB file..
Thanks,
Hi Jenny,
As you have a trigonal/hexagonal spacegroup, have you eliminated the
possibility of twinning? This can create ghosts in the density...
Cheers,
James
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