Dear Lothar
[I’ve copied this to the CCP4 team in case they have suggestions]
I don’t think there is any specific guidance for writing a “CCP4 program” - the
programs distributed in the suite have been written in a diversity of styles
and languages over many years - but I can offer a few
I am a structural biologist who is teaching X-ray crystallography. Recently I
noticed that BrlR structure (5XQL) was solved using molecular replacement with
a search model of very low similarity. I am very interested in this structure
because I think this a very good example to show students
Richard,
I can’t help you with 5XQL.
However, I can point out a recent structure from my group that might be useful
for teaching. The structure was solved by MR with a search model that had 33%
sequence identity and represented only 46% of the target structure. The Methods
section of the
On Tuesday, 18 July 2017 00:01:59 CDaddy wrote:
> I am a structural biologist who is teaching X-ray crystallography. Recently I
> noticed that BrlR structure (5XQL) was solved using molecular replacement
> with a search model of very low similarity. I am very interested in this
> structure
Hi all ,
It has been reported the Negative stain EM of a protein A-B complex, but
according to my gel filtration results (I purified A and B respectively for
incubation) , I found that A could not bind to B, of course I tried different
buffer condition with various pH value, even the binding
Hi,
This might indicate that the binding affinity of your complex is not high
enough for it to resist the gel filtration dilution. Maybe running a native
PAGE gel would allow you to visualise a complex.
Best
A
> On 18 Jul 2017, at 10:25, 高艺娜 wrote:
>
> Hi all ,
>
> It has
Dear Dr.Richard,
Your paper gave a good example for us.
Is it possible that you send me all the related files? It will be very helpful
for students to learn the detail of solving difficult protein structures.
Thanks in advance!
best,
Zhonghao Chen
China agricultural university.