What is the cell difference? Space group difference- surely not??? Between
the two data sets.
At lowish resolution the maps can tolerate more cel difference of course
than at high resolution..
Eleanor
On Wed, 21 Nov 2018 at 13:09, Almudena Ponce Salvatierra <
maps.fa...@gmail.com> wrote:
> Dear
Dear colleagues:
For those of you interested in cryo-EM, Matthijn Vos and I would like to
announce that we have just made a large set of new training videos public
covering the operation of Arctica and Titan Krios microscopes. The videos are
part of an ongoing expansion of the original “Getting
Dear all,
We have an opportunity for a Postdoctoral Scientist with an interest in protein
crystallography and fragment-based discovery to join the group of Prof Paul
Brennan, head of Chemistry at the ARUK Oxford Drug Discovery Institute (ODDI)
and the Structural Genomics Consortium (SGC). The p
Dear Pavel,
thanks for the quick reply. Indeed, when I place the ligand where I suspect
it could be, the program says: The polder map is likely to show the ligand.
Indeed I see a blob ...
I watched the video tutorial some time ago. It's very easy to use, indeed.
Concerning the Fobs-Fobs maps, th
Hi Almudena,
I wonder to which extent I can trust the positive blobs or polder maps that
> I am generating...
>
the answer to this question is given in corresponding paper that describes
Polder map:
http://journals.iucr.org/d/issues/2017/02/00/ba5254/ba5254.pdf
Based on the analysis described in
Dear all,
I have recently determined the structure of a protein for which useful data
extends to 4.2 angstroms (as assessed by paired refinement after pdb redo),
with some dazzling 80% solvent content and... I am expecting to find a
26-atom ligand bound to it. However the "blobbyness" of the maps
