Dear all just a reminder as this was posted during holiday period...we have a
vacancy for a 1 year post-doc at diamond which brings together crystallography,
2D-IR spectroscopy and biology. Full details in link below:
http://www.mis.strath.ac.uk/Personnel/open/r702011.htm
informal discussions
Hi,
I am facing some problems in solving my structure now, so I am wondering if
anyone is able to give me any tips and tricks on this matter.
My protein-DNA complex structure diffracted to 1.5A. There are 4 missing
residues, 2 on each terminal. There is no twinning in the data. The angles, the
Are you absolutely sure of the spacegroup?
Eleanor
On 09/13/2011 09:55 AM, #HEW KAI LI KELLY# wrote:
Hi,
I am facing some problems in solving my structure now, so I am wondering if
anyone is able to give me any tips and tricks on this matter.
My protein-DNA complex structure diffracted to
Hi there,
In crystallography there are so many places where you can have problems
(and need to solve these problems) that I cannot list them all.
There is no twinning in the data - you probably mean the data does
not seem to indicate the presence of twinning but there might be
twinning;
Any crystallographers here at Istanbul University ?
Dexter Kennedy, MD
Thumbed from my iPhone
On Tue, 2011-09-13 at 08:55 +, #HEW KAI LI KELLY# wrote:
However, Rfree refused to go down any further and it's still around
30-31%
And you have built the DNA already, right?
--
Oh, suddenly throwing a giraffe into a volcano to make water is crazy?
Hi all
Suppose you have a high resolution xtal structure (from usual x-ray
diffraction) and you wanted to verify the location of a ligand. You can
purchase a heavy atom isotope version of the ligand.
[1] Is it possible to do a neutron diffraction difference map (where you simply
calculated
