On behalf of Djemel Hamdane
Please find below a 2 years post-doc opportunity at College de France, Paris,
France, in the Djemel HAMDANE group in the Laboratoire de Chimie des Processus
Biologiques directed by Marc Fontecave
Hi Radu,
This may be caused by the coordinates being too many unit cells away from the
origin. In COOT you can easily ‘symmetry move coordinates here’ to a place
closer to the origin.
Hope this helps,
Robbie
Sent from my Windows 10 phone
Van:
Dear All,
Apologies for posting a Buster-related question to this list, the
buster-discuss one seems less active :-) I am trying to run a refinement job,
and hit the following problem:
ERROR : [run_buster-0046] unable to create initial SCREEN
output with gelly - see
Dear all,
We are pleased to announce coordinated upgrades to STARANISO for
analysis of anisotropy in diffraction data [1] and to autoPROC for
data processing and analysis [2].
The consistency between the two programs has been increased, so
has the uniformity of output. The final
This is not at all conclusive, but one depressing thing is that DNA-only
crystals are often hexagonal (like yours are).
Can you reproduce them without the protein?
++
Phoebe A. Rice
Dept. of Biochemistry & Molecular Biology
The University of Chicago
It’s been my experience that protein crystals with that high a percentage of
tryptophan residues (>2%) should give a very clearly positive result from a UV
microscope such as a Jansi UVEX.
Diana
**
Diana R. Tomchick
Professor
Departments of
Hi Robbie, Pietro,
Thank you for the quick replies! I tried this before, but must have messed up
things afterwards somehow... Anyway, tried again and now Buster works
beautifully. Indeed the molecule was a couple of unit cells away from the
origin, as the error message suggests... My fault.
Best
Dear Radu,
Nice to know that your problem is sorted and that you are pleased
with the results you are getting from BUSTER.
Clemens had drafted an answer along exactly the same lines and
circulated it around the team for comments, but we were momentarily
distracted by something else and
Dear Colleagues,
I would like to draw your attention to the 2-day Kendrew Symposium:
"Revolutions in Structural Biology: Celebrating the 100th Anniversary of
Sir John Kendrew" which will take place on 16-17 November 2017 at EMBL
Heidelberg.
The aim of this event is to celebrate Sir John
Dear Gerard,
Thank you for the answer, absolutely not a problem! I am very grateful for all
the great software from Global Phasing and I know that support is great.
Enjoying the STARANISO server for example atm.
Best wishes,
Radu
> Dear Radu,
> Nice to know that your problem is sorted
Dear Chris,
this is not an answer to your question but may be helpful anyway.
I checked your glycan with pdb-care at
http://www.glycosciences.de/tools/pdbcare/ and found what I already assumed
from looking at the image you had sent: Some of your residues feature a wrong
anomer. BMA303B is an
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