Hi folks
We are pleased to announce the release of iMosflm/Mosflm 7.1.3; if you are
collecting data on beamline I24 at Diamond using their new vertical goniostat,
you *must* use this version to process your data - see the release notes for
further details.
In addition to support for I24, the
Dear CCP4BB community,
we are pleased to announce that the period for applications to attend the
second edition of the INSTRUCT-COST Training Course ISBio2015
http://xtal.dq.fct.unl.pt/PosterISBio-2015.pdf is open until June 15.
Integrative Structural Biology tools for the study of
The EPSRC Centre for Doctoral Training in Cross-Disciplinary Approaches to
Non-Equilibrium Systems (CANES) has two fully-funded four-year PhD projects
that are co-sponsored by the National Physical Laboratory for Sept. 2015 entry:
1) De novo peptide self-assembly for antimicrobial and gene
On 19/02/15 21:03, Phoebe A. Rice wrote:
When trying to adjust the chi angles of a dT in coot 0.8.1, the
methyl and its H's (which I called C5M to make phenix happy) rotate
with the sugar, producing a rather base bizarre geometry.
Hello Phoebe,
I suspect things are going wrong because C7
Ursula,
Most compounds used for cryosolutions glycerol, ethylene glycol, propane
diol increase protein solubility.
A warning, these compounds are also hygroscopic, you need to change your
vapour diffusion methodology.
Vera L., Czarny B., Georgiadis D., Dive V., Stura E.A. (2011) Practical
Hi,
I’d like to bring the following position into the attention of any suitable
candidates:
-
POSTDOCTORAL POSITION IN MOLECULAR MATERIALS RESEARCH, UNIVERSITY OF OULU,
FINLAND
A two-year interdisciplinary postdoctoral position in molecular materials
research is available in the Research
Thank you for the multiple kind off-list responses I received regarding how
to interpret map colors in Coot. I'm very grateful for the references, but
it seems that I did not state my issue clearly :-) What I was referring to
was the tool that Coot has under Validate Density Fit analysis. The
On 19/02/15 11:00, Emilia C. Arturo (Emily) wrote:
Hello all.
Hello Emilia (Emily),
I'd like to understand what it is I'm looking at when I use Coot's
density fit analysis tool. I recognize that there was a post related
to this topic on the Coot bb a while ago --the discussion was on how
On Fri, 20 Feb 2015 16:07:18 +0100, Pietro Roversi
pietro.rove...@bioch.ox.ac.uk wrote:
Dear Enrico,
I wonder if trying different protein:precipitant ratio is also a valid
strategy to crystallise very soluble proteins.
Please let me know if my reasoning is flawed and if so why!
Yes and
Dear CCP4bb readers,
a PhD position (starting in October 2015) is available in my laboratory
(www.icr.ac.uk/alessandrovannini) at The Institute of Cancer Research (ICR,
Chelsea, London, UK), to undertake crystallographic, single particle electron
microscopy analysis and biochemical analysis of
I use a syringe with a needle and poke through the tape into the
reservoir and top it off
Another approach is to poke holes in the tape with a needle, and just let
the drops slowly evaporate and dry out. I'm told it works!
On 17 February 2015 at 09:19, Bernhard Rupp hofkristall...@gmail.com
Just recently, we updated Coot to use the Ramachandran plot according to
some newer distribution as defined by MolProbity (thanks to Kevin
Cowtan's clipper). This is available from Coot rev 5581.
However, please keep in mind as pointed out by Gert that there are
different version of the
To those in the same spot, the fix was to first run this:
http://kinemage.biochem.duke.edu/software/remediator.php
And then remove all the H's and let your favorite refinement software put them
back:
grep -v H 52remediated.pdb 52remediated_noH.pdb
Sorry for bothering those of you who
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