Hi everyone,
I met a problem when trying to build ideal DNA model in Coot. The
calculated DNA looks less than 10.5 bp/ turn, probably is about 10 bp/
turn. Is there a way for me to change the pitch to make it 10.5 bp/turn in
Coot?
Thanks for your kind help!
Sincerely,
Frank
Dear CCP4 Users
A CCP4 update has just been released, consisting of the following changes.
* QtRView: corrected Prosmart result page; enabled incorporation of web-links
into citation section
If you do not currently receive updates, consider re-installing your
CCP4 setup using the latest binary
Applications from potential PhD students, post-doctoral fellows, and research
technicians are invited for the protein X-ray crystallography group at Trinity
College Dublin, Ireland. The projects are diverse and involve the
crystallization of bacterial/cellular protein complexes associated with
Dear Colleagues,
We hope that you are planning to attend the International Conference on
Structural Genomics 2013, which will be held in Sapporo, Hokkaido, Japan, July
29th – August 1st, 2013. ICSG2013-SLS is intended to provide an overview for
the most recent developments in Structural Genomic
A good starting place:
Biophys J. 1996 Oct;71(4):2049-55.
Evaluation of linked protonation effects in protein binding reactions using
isothermal titration calorimetry.
Baker BM, Murphy KP.
Abstract
A theoretical development in the evaluation of proton linkage in protein
binding reactions by iso
Dear colleagues:
I was wondering if you could kindly share your thoughts and help me
understand the relationship between pKa and affinity of a protein for a
ligand. Are these two properties related? Specifically, does a lysine with
a pKa of 8.5 have a greater affinity for a negatively charged liga
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Hi Ed,
I guess your criticism is adequate - I'll stop doing this. My
apologies to Eugene.
Best,
Tim
On 04/04/2013 02:43 PM, Ed Pozharski wrote:
> On 04/04/2013 04:29 AM, Tim Gruene wrote:
>> Dear --,
> Are we, the "ccp4bb community", recently on the
On 04/04/2013 04:29 AM, Tim Gruene wrote:
Dear --,
Are we, the "ccp4bb community", recently on the hunt to find new and
exciting ways to make sure people stop asking questions? Gentleman from
Moscow has clearly disclosed his full name and affiliation, but perhaps
I am wrong and subtle critici
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Dear --,
you also see the molecule ID in the status bar which matches the ID
within the Display Manager Window which in turn shows the name of the
structure file you loaded.
Best,
Tim
On 04/04/2013 10:24 AM, Evgeny Osipov wrote:
> Hello everybody, I
Hello everybody,
I have a question about structures comparison in coot 0.7
After aligment I pick up one residue and see only atom name, residue
number and chain identifier in status bar. Is there any way to see exact
name of molecule ?
Example: structures with pdb 3pps and 2q9o were loaded and
Hi Francois,
add the keyword "JOBS N" to your scripts. If it still uses more than N
threads, this is possibly a bug.
BW, Gabor
On Apr 4 2013, Francois Berenger wrote:
Hello,
Is there a way to tell the new phaser to not
use more than N threads when running?
I have a problem with it overloa
This is a reminder of the announcement of the Data Collection Workshop,
which will take place at the BESSY II synchrotron in Berlin from June
13-15, 2013.
There is only about 10 days left to the deadline.
For details concerning the program, please see:
http://www.helmholtz-berlin.de/bessy-mx-wo
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