>
> On Mon, Jan 26, 2015 at 8:22 PM, Monica Mittal
> wrote:
>
>> Hi everyone,
>>
>> I need an advice on some strange thing happening to one of the protein i
>> am working on. I used to purify it and set up trays and get some needle
>> shaped crystals and trying seeding and other methods to optimis
Hi,
It happened with me also, thought I had not the needles but the crystals.
Temperature matters a lot in these situations, leave the trays unattended
for long and also try with various concentration. Make it highest say 15
mg/ml and dilute serially to set with a range of concentrations. Sometime
Thank you, Rachel. I will try this suggestion out. -Original Message-From: kra...@rcsb.rutgers.eduSent: Mon, 26 Jan 2015 09:22:00 -0700To: patrick.coss...@inbox.comSubject: Re: [ccp4bb] extracting PHENIX structures (help-6435)
Dear Patrick,
You can try to write a scrip
REMINDER: Call for access to Synchrotron Beamline Facilities, 2015 -
EMBL Hamburg, Germany
We would like to remind you of the approaching deadline (*Saturday 31st
**January 2015*) for the call for proposals for synchrotron beamline
applications at EMBL Hamburg.
The call is for applications i
Hi all,
This is just a quick reminder that the application period for our 3 vacancies
is closing this Friday at midnight. We are seeking to recruit:
- two curators (PDB/EMDB) -
http://ig14.i-grasp.com//fe/tpl_embl01.asp?newms=jj&id=53264&aid=15470
- one web front-end developer -
http://ig1
Dear all,
A quick question regarding the density modification interface via the
Sharp interface. Which resolution range / radius of the solvent sphere/
ncycles should be used for optimal result?
The documentation seems to suggest to restrict yourself up to the
resolution where good phasing inf
Hi everyone,
I need an advice on some strange thing happening to one of the protein i am
working on. I used to purify it and set up trays and get some needle shaped
crystals and trying seeding and other methods to optimise them. But
recently, it stopped giving crystals even small needles. I am sti
Dear Jeorge,
you'll find some information about this in
http://strucbio.biologie.uni-konstanz.de/xdswiki/index.php/Space_group_determination
. A practical and easy way is described in
http://strucbio.biologie.uni-konstanz.de/xdswiki/index.php/Pointless
HTH,
Kay
On Mon, 26 Jan 2015 11:24:27
Dear Jeorge,
XDS make no claim to determine the SPACE GROUP but rather the LAUE
GROUP, as only the latter is taken into account during data integration.
This is definitely so during the indexing step (IDXREF.LP), but even in
CORRECT, when systematic absences are sometimes indicated, XDS does not
Dear CCP4 members,
I’m working on a phosphocholination pathway in which the enzyme utilizes the
substrate Cytidine-diphosphate-choline (CDP-choline) as phosphocholione-donor.
I’m enquiring about the possible analogs of CDP-choloine for
cocrystallization with the enzyme as well as for the inh
Hi Robbie,
thanks a lot. I was suspecting that editing the PDB was probably the
easiest way to go. I will try that!
Best,
Almudena
2015-01-26 10:44 GMT+01:00 Robbie P. Joosten :
> Hi Almudena,
>
> You can use Cootilus/Nautilus to rebuild the nucleic acid in your current
> density. This is not
Dear all,
Please find attached a post doc offer to study cytoskeletal septins by electron
microscopy.
The project will be carried out at Institut curie (Paris).
Someone with a former experience in electron microscopy or willing to be
trained in EM is encouraged to apply.
Best regards
A.Bertin
**
Hi Almudena,
You can use Cootilus/Nautilus to rebuild the nucleic acid in your
current density. This is not a direct conversion, but it should be quick
enough.
The conversion form RNA to DNA can be done (outside COOT) in a text
editor by changing the residue names an deleting the O2' atoms. If
Dear George and Patrick,
It is particularly tricky to do such a search for SHELX because there
are different ways of referencing it for refinement (SHELX, SHELX-76,
SHELXL, SHELXL-97, SHELXL-2014 etc.) and there are other ways of using
SHELX, in particular SHELXD for finding the heavy atom sub
Dear Jeorge,
I can’t see anything in that output saying whether the systematic absences that
would allow you to detect screw axes were covered in your data collection.
In any case, it’s not necessary to reintegrate. All that happens when going
from P222 to any one of the other 7 possible ortho
Dear all,
is there a "fast" way of changing the chain type from RNA to DNA or from
DNA to RNA within coot? I have already quite a bit built into density, but
it is the wrong kind of nucleic acid.
Best,
Almudena
--
Almudena Ponce-Salvatierra
Macromolecular crystallography and Nucleic acid chemi
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