I remember we discussed this a lot about a year ago when Ed Berry revived a
thread from 2003!
https://www.jiscmail.ac.uk/cgi-bin/wa-jisc.exe?A2=ind1905&L=CCP4BB&O=D&P=72099
I think the upshot of it all was that you do not need to use shells even with
quite high NCS since Ian Tickle rightly pers
On 15/06/2020 22:06, Cygler, Miroslaw wrote:
Hi
Hi.
I just started using coot 0.9 and see some differences in behaviour
from version 0.8. When I move to the next residue using space bar the
residue name of the residue does not appear. How can I make appear
automatically?
Wow, 0.8 and 0.9
Hi,
I just started using coot 0.9 and see some differences in behaviour from
version 0.8. When I move to the next residue using space bar the residue name
of the residue does not appear. How can I make appear automatically?
Best,
Mirek
Hi Joao
The top of the page was cut off in your screenshot so I can't see the
command line you typed. It would be better to copy/paste the entire text,
including the input command line and the output, into the email rather than
taking a screenshot. 'Cannot open file' most likely means that the i
Hmm - this finally was rather deprecated - there are some less happy
consequences to have all reflections in a particular resolution shell
excluded.
If your NCS means there is pseudo- symmetry in the diffraction and it would
be possible to have a cell with higher point symmetry (an example might be
Hello,
I'm refining protein structure in Refmac and I have NCS greater than 4 ( I've 8
identical subunits in the asymmetric unit).
In the "Refinement parameters" section in Refmac, how can I pick Rfree set
based on thin resolution shells rather than in the normal random method?
I've read abou
Hi Joao
For all CCP4 programs you need to source your CCP4 setup script.
Cheers
-- Ian
On Mon, 15 Jun 2020 at 15:29, Joao Ramos wrote:
> Dear CCP4bb,
>
> I'm trying to obtain RSC metrics using the CCP4 program EDSTATS for a
> Phenix refinement job, in order to have a more reliable analysis o
Dear CCP4bb,
I'm trying to obtain RSC metrics using the CCP4 program EDSTATS for a
Phenix refinement job, in order to have a more reliable analysis of model
quality. From what I read, one should go through the program MTZFIX and
then create the FFT maps (density and difference maps). However, whil
Last chance to register:
Cryo-EM for Drug Discovery | June 16, 2020
What if you could get structural insights at near-atomic resolution of
your most challenging drug targets at a pace that meets that of your
drug discovery projects?
>From around the world you are invited to join Thermo Fisher
Dear colleagues,
Please pass this along any one who might be interested. Thanks!
/Bjørn
STRUCTURAL AND FUNCTIONAL STUDIES of eukaryotic membrane proteins involved
in sterol transport
(http://pedersenlab.dk/source/phd_position_2020.pdf)
A PhD posit
Why not just use QTMG rather than Pymol? This is, after all, the _CCP4_
bulletin board…
H
> On 14 Jun 2020, at 23:56, Javier Gonzalez wrote:
>
> Thank you so much Vijaykumar and Kevin, it worked smoothly!
> Best wishes,
> Javier
>
> On Sun, Jun 14, 2020 at 5:04 PM Kevin Jin wrote:
> My OS Ve
11 matches
Mail list logo
