Dear all,
We work with lipid droplet binding proteins in our group. These
proteins behave more like membrane associated proteins, have a very hydrophobic
surface and require detergents right from solubilization to crytallization.
We use 1% DDM for solubilization, 0.03% DDM t
Hi All,
We are seeking highly motivated individuals to fill in postdoctoral
positions to study structures and functions of proteins and protein
complexes involved in assembly and genome packaging of complex DNA
viruses such as human herpesviruses and bacteriophages by means of X-ray
crystallo
There is a DVD available now by Juan-Manuel Garcia Ruiz.
I previewed it at the ECM in Darmstadt - very impressive and
better science than the Nat Geo flick.
http://tinyurl.com/286su7w
BR
-Original Message-
From: Bernhard Rupp (Hofkristallrat a.D.) [mailto:hofkristall...@gmail.com]
Sent:
Fulvio,
We need more info to give advice. First, when you say Rsym is 0.18,
are you talking about in the high res bin or overall? Second, how did
you determine you have twinning? In what space group did you scale your
data? If your data is actually twinned with a high twin fraction, and
yo
It may be time for our annual I/sigmaI discussion.
Please note that is what the RCSB expects from you and it is
generally lower than /. Some packages do not output
in an obvious place for you to put in your Table 1. :)
On Wed, 6 Oct 2010, Ed Pozharski wrote:
You don't need twinning to
You don't need twinning to invalidate the Rmerge as a criterion for the
resolution cutoff, there are other reasons why you should use I/sigma
instead. If you process data all the way to 3A, what's the I/sigma in
the highest resolution shell?
On Wed, 2010-10-06 at 11:28 +0200, fulvio saccoccia wr
Dear All,
I have just installed the current CCP4 dmgs onto a Macbook pro, and everything
seems to be OK.
However, on running amore from ccp4i, in the initial sorting and tabling steps,
the sorting works fine, but the tabling step does not run at all - i.e it is
not called from the gui interfac
I recently got the 24 inch Zalman and when the coot window is
maximized the 3D is reversed. I know I can minimize it slightly and
move it up and down a pixel to fix it. Has anyone found a trick to
leave it maximized and correct the 3D. I have tried adjusting screen
position but have not foun
Dear all,
I have a data set collected at 3A resolution. I processed the data but I
had to cut the resolution at 3.6A for the high value of Rmerge (at 3.6A
it is 0.18). After scaling and MR I realized that my data were twinned.
This is my question: can I reprocess all the data set using all the
On 01/10/10 16:57, Sickmier, Allen wrote:
I recently got the 24 inch Zalman and when the coot window is
maximized the 3D is reversed. I know I can minimize it slightly and
move it up and down a pixel to fix it. Has anyone found a trick to
leave it maximized and correct the 3D. I have tried
Hello,
I am surprised to hear that it is difficult to get hold of Zalmans, so I spoke
to a person from alternate this morning.
At least people within Europe they are avaible and on stock (see
www.alternate.eu)
For people in the US, I am afraid, you would have to contact them directly -
according
If u have external emitter controller then just press the "reverse"
button .. thats how I solved this problem, but i use CRT
monitor with Nvidia card in RHEL WS4.
Cheers,
Amit Das.
--
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AMIT DAS
PROTEIN CRYSTALLOGRAPHY
SO
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