Are you certain that the data are not twinned?
HTH
Kay
Dear Dilip Badjugar,
Perhaps it may be good to take a look at the unmodelled blobs and see if
there is any large densities left unexplained.
Also how does the Rmerge vary with the resoln ? Is your data good upto
1.7A?
Regards and wishes
Krishnaswamy
On 13 Oct 2013 04:33, "CCP4BB automatic digest
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Dear DCB,
do not look at the R-values too much, look at your structure and your
maps. If they look as though you cannot improve the model any further,
accept that the R1/Rfree are 21% and 25% - at 1.7A resolution these
values are acceptable. Go publis
Hello Experts,
I am trying to solve structure of a protein (213 a.a) complexed with a
peptide (14mer) using molecular replacement method. The complex crystals
are diffracted around 1.7 A and data is processed in p3(2)21 space group.
The structure was solved using apo protein with good LLG -3148
For your consideration:
Celebrating Crystalllography — a short film made by the Royal Institution (in
cahoots with production company 12foot6) and funded by the STFC.
http://richannel.org/celebrating-crystallography
