Hi Yahui, using a text editor like Mac TextEdit you can also click the option
key (cursor will change to cross shape), click and drag to select column, copy
and paste.
All the best,John
On Monday, January 13, 2025 at 09:02:49 AM CST, Hui YAN
wrote:
Happy New Year, everyone!
I am look
Hi there, all good suggestions to optimize crystals, here are few other things
to try:
1. Spin down your protein sample in a centrifuge prior to setting up trays to
remove protein aggregates.2. Incubate trays at lower temperatures (for example
if crystals grow at RT, try 15 and 4 C).3. Try stre
s
> more accurate results, but may use more computing time.
>
> Hope this helps,
> Kay
>
> On Sat, 5 Oct 2024 13:45:59 +, John Bacik wrote:
>
> > Dear Kay, do have any more information or would you mind explaining a
> bit more what changes in the XDS code led to
Dear Kay, do have any more information or would you mind explaining a bit more
what changes in the XDS code led to these significantly different statistics in
the different XDS versions?
Thanks,John
On Wednesday, October 2, 2024 at 02:35:25 PM CDT, Kay Diederichs
wrote:
Dear Yimin,
lletin board
on behalf of John Bacik
<b45abf420e1f-dmarc-requ...@jiscmail.ac.uk>
Sent: Friday, July 26, 2024 11:18 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Presence of negative density in Sim Omit map
| | You don't often get email from
b45abf420e1f-dmarc-requ...@jis
Green
StreetUniversity of GeorgiaAthens, GA 30602Tel: (706) 583 0303From: CCP4
bulletin board on behalf of John Bacik
<b45abf420e1f-dmarc-requ...@jiscmail.ac.uk>
Sent: Thursday, July 25, 2024 12:21 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Presence of negative density in
o localized
around the peak -
depending on your low-res cutoff. As John Bacik suggested you should check for
a mis-modeled part of
a symm-related molecule, but if that were the case, you should see the red
density even before
omitting the loop, and you should see the red density somewhere
Hi Renu, you may try using a Polder omit map for the region rather than a
simulated annealing map. You may also check if the red density is due to a
symmetry related molecule that is not modeled well. Hope it helps.
JP
On Tuesday, July 23, 2024 at 04:50:00 PM CDT, Renuka Kadirvelraj
Hi Gottfried, I was wondering what happens if you make a Polder omit map for
the HEPES? I am also curious, if the extra positive density is for missing bulk
solvent with ligand of occupany 0.5, do you observe the density with ligand
present at 0.5 occupancy to be more diffuse than with no liga
Hi Devbrat, here are a couple of other things to try:
- When screening crystals use rastering to find regions of the sample where
multiple lattices may be less problematic. If multiple lattices are observed,
often regions on the crystal(s) close to the edge will not be as affected by
twinning/
http://lansce.lanl.gov/lujan/instruments/PCS.shtml.
We strongly encourage you to contact us for questions concerning sample
preparation, instrument capabilities, sample environments, and/or proposal
preparation.
Julian Chen, che...@lanl.gov
John Bacik, jba...@lanl.gov
Clifford Unkefer, c
Hi Shivesh,
Have you tried dropping your MPD concentration (ie. by increments of
~5%)? Changing the pH may also result in larger crystals.
JP
On 1/30/07, shivesh kumar <[EMAIL PROTECTED]> wrote:
Dear all
Sorry for unrelated query.I have crystallized a protein which is at 40% of
MPD.But the p
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