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*Macromolecular Crystallography, Biophysics and Biochemistry*
Two post-doctoral fellowship positions are available at the University of
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Dear all,
a postdoc position is available now at the Clare Hall laboratories, London
Research Institute, Cancer Research UK.
Best
Alessandro
About the job
A postdoctoral position is available at the Clare Hall Laboratories, Cancer
Research UK, in the research team of Dr. Alessandro Costa.
Maybe try CNS or SFCheck:
http://groups.yahoo.com/neo/groups/cnsbb/conversations/messages/1720
To improve Phenix maps, maybe try increasing the number of boxes (the
parameter IIRC "n_box_target=" )
http://www.phenix-online.org/documentation/autobuild.htm
In CNS, you can decrease the starting temp
I have two bits of advice.
1. If the SA omit map for the ssDNA is "really bad", perhaps you should
reconsider whether your model is a faithful representation of the experimental
data.
2. You could use anomalous difference Fourier analysis to locate the P atoms of
the DNA backbone. We did thi
Hi Deng -
Can you tell why the reviewer was asking for the SA-omit map? Is there
some doubt about the conformation of your ssDNA, or even whether it is
present in the first place? Is there a question about the sequence, or
the sequence register (which nucleotides go in which positions)?
Ev
Hi Deng,
> Recently, I received the comments from referees, they asked for the
> SA-omit map of the ssDNA of our protein-DNA complex. They said that simulated
> annealing omit map better than a biased 2Fo-Fc. The ssDNA consists of seven
> thymidine nucleotide. Our data diffracted to 2.65A,but th
Thanks Bernhard
you have helpfully distinguished between the two processes - there is
certainly a movement of waters to symmetry replacements closer to a chain - and
that gets documented in Remark 525 of the PDB file returned to authors -
although then it is stripped out, I think, before the
As far as confusion as a result of PDB renumbering is concerned: It was
useful to run the old REM525 standalone program (I think I got it from
PDBe/Kim Hendrick) at the end of solvent building. It does what the PDB did
with water renumbering when creating the REMARK 525 (probably based on ccp4
cont
Dear all,
Some of you might be interested in our international conference
"Membranes and Modules" which takes place in Berlin from March 26-29,
2014. We have a fantastic list of speakers with many structural biology
talks around the topics of protein quality control, plasma membrane
scaffold
Thank you for that, Rachel
Even though the tone of your comment does not suggest that you want to carry on
a dialogue about this, I thought I would reply in any case - since dialogue is
what this forum is supposed to be about.
Thing is, I was sort of looking for an explanation of why the rule
Dear Colleagues, I want to bring this position to your attention:
Faculty Position in Structural Biology
Purdue University
The Department of Biological Sciences and the Markey Center for Structural
Biology at Purdue University invite applications for a tenure-track faculty
position in Structura
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Dear zq Deng,
you may actually have some anomalous signal from the P-atoms in your
structure, even if you collected at short wavelength - if you have a
data set collected at, say, 1.5A, it would be even stronger.
In that case you could create an anom
What does a straight difference map look like? i.e. omit one nucleotide at a
time, do a few cycles of refinement and then inspect the weighted difference
map - SA may be too violent for your structure.
Eleanor
On 4 Nov 2013, at 06:36, dengzq1987 wrote:
> Dear all,
>
> Recently, I received th
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