I'm wondering if anyone has any still-functioning heated goniometer heads
that they no longer need. If so, please let me know offline from the list.
Thanks,
Chris
__
DR. CHRISTOPHER A. WADDLING, PHD
Crystallography Facility Manager
University of California,
I put some pictures of scattering from random things (including "air") here:
http://bl831.als.lbl.gov/~jamesh/pickup/images/
It is actually more difficult than you might think to get a clean image of
"air scatter" on a well-maintained camera. This is because we usually try
to minimize the contr
Dear Zhizhi,
we had a case like that. I would switch to slightly different buffer
(e.g. different pH) so crystals do not appear overnight, and then do
crystallisation screening. I bet you will have many hits in different
conditions, likely with bigger crystals.
Good luck!
Best wishes,
Tomas
On
Hi all,
After I purified my target protein by ion exchange, I left the fractions
with high protein concentrations overnight @4C. Now I saw a lot of small needle
crystals inside the EP tubes this morning.
I wonder whether there is any technique or method to get bigger crystals from
this?
ZZ
An easy example is heterotrimeric G-proteins. In the termination cycle, G-alpha
bound to GTP will hydrolyze the GTP, which then allows it to associate again
with the G-beta/G-gamma dimer.
Many membrane receptors (GPCRs, Chemotaxis, etc) can oligomerize and can be
viewed like this, i.e., one dim
Dear all,
Thanks again for all the suggestions.
I should perhaps add that I am working on glycosylated proteins and they
which tend to be quite flexible in some areas.
The website suggested by Ethan:
http://skuld.bmsc.washington.edu/parvati
did not show any areas that appeared alarming, or at
Hi CCP4BB members,
I was wondering if anyone knows of examples of 3-way obligatory associating
complexes. In other words, instead of having protein A binding to protein B
and protein B also binding to protein C, example of complexes where protein
C binds ONLY when proteins A and B are already asso
Hi Shiva,
There are some other enzyme systems activated by ligand induced oligomerization
in addition to the ones on this list:
1) DNA polymerase dimerization on DNA binding
2) Restriction enzyme dimerization on DNA binding (an example is the type IIs
FokI)
3) membrane enzyme receptors like rec
Dear All,
Thank you for your responses. Below is the compiled list of examples of
substrate/ligand/co-factor induced oligomerization:
http://www.pnas.org/content/97/13/7096.full.pdf
http://www.ncbi.nlm.nih.gov/pubmed/15710608
http://www.ncbi.nlm.nih.gov/pubmed/17725819
http://www.ncbi.nlm.nih.gov/
Hi Tim,
no, in the cases I remember there was no significant difference in geometry -
of course, we do tend to work on rather stable, rocky proteins...
Mark
On 9 Aug 2013, at 16:33, Tim Gruene wrote:
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> Hi Mark,
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> does your experience also
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Hi Mark,
does your experience also include the geometry of the model? There
might be improvements, as e.g. reported from molprobity, because of a
better modelling of the temperature factors.
I am asking because you mention improvements of the electro
Omid,
how necessary is it that you do TLS refinement? I.e. are you just doing it to
improve your Rs a bit or is the density really getting better? If the density
is not improving, I would just refine without TLS and avoid any posterior
temperature factor analysis difficulties.
While I am sure th
Dear all,
the integrated facility at EMBL Hamburg at the PETRA3
synchrotron in Germany consists of two macromolecular crystallography
beamlines, a BioSAXS beamline and a laboratory for sample preparation and
characterization. For those of you who are interested in a comprehensive
characterizatio
If you are willing to include cofactor-induced oligomerization instead of
substrate-induced, how about imidazoleglycerol-phosphate dehydratase (IGPD) ?
Inactive trimer: 1RHY
http://www.ncbi.nlm.nih.gov/pubmed/14724278
Active 24-mer in presence of Mn2+ ions: 2F1D
http://www.ncbi.nlm.nih.go
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