In situations like this I always try dropping to P1. Even if the data
are highly incomplete in P1 you can still refine it. Difference maps are
degraded by poor completeness, but you still might see something. But
either way, the R-factors will tell you something. if dropping to P1
solves
thanks. Coot works!
On Wed, Apr 19, 2017 at 10:20 AM, Vipul Panchal
wrote:
> I am not experienced with pymol. However if you are familiarized with
> coot, you can mutate and set rotamer. It is really simple.
>
> On 12-Apr-2017 12:15 AM, "Alex Lee"
We have an ADSC Q4 system and a Q4R system that we no longer need.The
detectors have not been used for several years and have probably lost vacuum
and therefore need recalibration. In the likely event that no-one wants the
entire system we will split it up for those who want parts such
Just a quick remainder.
Last Five days for the low-rate registration at the 6th International School
on Biological Crystallization (ISBC2017).
May 29th to Jun 02nd.
For more information, please visit http://www.isbcgranada.org/.
Best regards,
ISBC 2017
Hi Abhishek
Im by far not as experienced as others in the bulletin board, but I made the
experience that automated water update with Phenix leads to an aggressive
placement of solvent molecules, which can be damped a bit by restricting H-bond
distances of newly placed waters. As Robbie and