Dear all,
on behalf of Dr. Dmitri Svergun, I would like to draw your attention to
the following EMBO Global funded course
that we will host together with Prof. Cristiano Luis Pinto de Oliveria
in **São Paulo** in January 2014.
regards
Margret
VACANCY - (SENIOR) POSTDOCTORAL RESEARCHER IN GENE EXPRESSION FOR
STRUCTURAL GLYCOBIOLOGY, University of York, UK
We wish to appoint a postdoctoral researcher to work on the expression of
mammalian genes, for 3-D structural and chemical mechanistic studies, in
the area of eukaryotic glycobiology
Posted on behalf of Dr. A. Vale (avale_at_ibmc.up.pt), to whom all
enquiries must be directed.
The Fish Immunology and Vaccinology Group of Instituto de Biologia
Molecular e Celular (Porto, Portugal) is seeking for a Post-Doc to work in
the project “Studies towards identification of structural
Many thanks to all of you for useful links and suggestions.
Best regards...
Hena
On Wed, Jul 24, 2013 at 7:51 PM, Bostjan Kobe b.k...@uq.edu.au wrote:
Hena
I agree with the responses so far, but I think It may not be a complete
waste of time looking at the crystallization conditions for
Thurs. July 25th, 2013
EBI
also an interesting article on the subject of women in science then and
today
http://www.guardian.co.uk/technology/2013/jul/25/rosalind-franklin-google-doodle
Miri Hirshberg, PDBe
On Thu, 25 Jul 2013, David Schuller wrote:
Dear all,
I would like to thank everyone for being so kind and sparing their time to
respond. Just to summarise from all the responses that I got that may help
someone else:
MBP on its own is monomeric and tends to 'magically' help pretty much every
protein you throw at it to become soluble. In
Hi all,
I'm working with a protein that appears to be a dimer in solution, on
SEC in runs as 24 kDa, while the actual mass of a dimer is 30. And I am
trying to figure out which dimer is the biological one (it is a
regulatory protein but details are uknown). The crystal structure gives
me a
Hi Karolina,
You have an interesting case in hand but which is not uncommon. From your description it sounds as if option 2 is more likely to represent the biological dimer but as you noted, it's not certain. Best would be to obtain another crystal form (easily said,
I know, not easily
Hi Karolina,
I would suggest you do SAXS. You can compare the
scattering profile you get from your protein in solution to the calculated
profiles of the three possible dimers (or other oligomers) you have in the
crystal structure. This should give you a definitive answer. See for
example this
Hi All,
I am wondering if I can fix a set of selected atoms during simulated annealing
in phenix.refine?
I only found the option in xyz refinement, but not in annnealing.
Thank you!
Hi,
I am wondering if I can fix a set of selected atoms during simulated
annealing in phenix.refine?
no.
Pavel
P.S.: There is Phenix mailing list for Phenix-specific questions
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