PhD (CIFRE) position – SANOFI & ESRF on cryoEM methods applied to antibodies
PhD thesis title: High resolution Cryo- Electron Microscopy of Antibody /
Antigen complexes
More and more research focus is being put on biologics and their development as
drugs. These molecules are usually large and
On 01/06/2017 23:39, Ursula Schulze-Gahmen wrote:
Does anybody know how to turn off the molprobity probe clashes in the stand-alone version of
Coot? I just turned them on and now I seem to be stuck with them.
Draw -> Generic Display Objects -> Undisplay All
or Delete the if you wish.
Paul.
Does anybody know how to turn off the molprobity probe clashes in the
stand-alone version of Coot? I just turned them on and now I seem to be
stuck with them.
Ursula
--
Ursula Schulze-Gahmen, Ph.D.
Project Scientist
UC Berkeley, QB3
360 Stanley Hall #3220
Berkeley, CA 94720-3220
(510) 643 9491
Dear All,
A short-term (maternity cover) postdoctoral position is available in
protein X-ray crystallography on a drug discovery project at King's
College London (Guy's campus, London, UK).
The following link contains further information about the post, and
details on how to apply:
Dear colleagues,
Please see the information below regarding an opening in our research group.
Please share with anyone who might be interested.
Best regards,
-Joseph.
A two-year post-doctoral position is available at the Department of Medical
Biochemistry and Biophysics
Vincent,I see a few of problems with your SRF (the maps) which would impact the interpretation. First you say that both crystals are processed as P21, which you would expect a very strong peak (100% of your origin peak) on kappa/chi=180 at the b* axis (one of the major axes of your map); this
Thank you for your email.
the anisotropic resolutions of the datasets are 5.6-7.1A for the best
and worst diffracting directions of the crystal without additive, and
4.0-5.8A for the crystal with additive.
The two crystals come from the same prep and same drop setup, only
differ from the
