Dear all,
I have just received response from the PDBj Annotator through CCP4BB
My PDBs will be processed within two weeks
As some of you mentioned, the reasons of delaying processing time is due to
holiday season and the extremely large amount of depositions recently
Again, thank you
Dear all,
Thank to your replies, I am so released now!
Thank you a lot for all responses.
Best regards.
Dear all,
Last year, when I deposited PDBs using ADIT, immediately I got an automatic
confirmation email. And after 1 day, I got the responses from the PDBj
Annotator. And within 3 days, all the edition and validation of my structures
were finished with the help of member from the wwPDB. I g
Hi Neeraj,
A few points to add to Artem's excellent advice:
If you would like to purify an untagged construct of your kinase, you could try
an ATP affinity column. The caveats to this are 1.) the ATP resins can be
expensive, and therefore it may be impractical to make a column with a high
bind
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adv
Especially if you're dealing with lysate, I suspect the best way to do it is
with magnetic Ni beads that you lift up and out of the gunk, to help avoid
false positives from aggregating stuff that SDS/urea/guan would all "elute".
But why do you want X to remain on the column/beads? Removing Y bu
That's great. The 3D screen we got is only 23 inch. A full screen GUI
like in the game will certainly be helpful.
Nian Huang, Ph.D.
Dept of Biochemistry
UT Southwestern Medical Center
Dallas, TX 75390
On Fri, Dec 31, 2010 at 5:00 PM, Nian Huang wrote:
> Dear all,
> The python version coot has tw
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