An immediate position is available for up to 5 years for an enthusiastic and
highly motivated postdoctoral Research Associate in the area of Outer Membrane
Uptake of Antibiotics. You will participate in a European consortium
(TRANSLOCATION) consisting of academic labs, small biotech firms and
Hi Wei,
If you have an interpretable density, the efficientest way in my
opinion, is to construct manually (only 6bp).
You can use coot and the button add residue. Coot can add nucleotide
directly at the extremity of your existing nucleic acid model.
Hope to help you.
Nicolas
Le 18/03/13
Dear All,
Firstly, thanks Ian and Michael's efforts on this issue and everyone's. We
pointed the space group to P43212, then it works okay.
Best Wishes,
Gengxiang
On Fri, Mar 15, 2013 at 1:26 PM, Ian Tickle ianj...@gmail.com wrote:
Michael, yes sorry I had (temporarily) forgotten about
Dear List,
Does anyone know of a source of quantification of membrane proteins in
garden-variety eukaryotic cell lines, e.g. HEK or HeLa cells (incidentally,
it just occurred to me that probably all HeLa cells are XX--seems right,
no?) I am looking for the highest-expressed, particularly, and
Dear all,
kind reminder for the International PhD program at the IGBMC, notably for
integrated structural biology,
with a deadline for applications 22nd of march 2013:
http://phdprogramme.igbmc.fr/
see also http://www.igbmc.fr/research/department/3/
Best regards,
Bruno Klaholz
In the mitocondrial inner membrane (which is very protein-dense) I believe the most abundant protein is the adenine
nucleotide transporter. (e.g. pdb1OKC). Single chain or homodimer, but apparently its not very easy to crystallize.
Jacob Keller wrote:
Dear List,
Does anyone know of a source
I don't want to crystallize the protein--I have another reason
Jacob
On Mon, Mar 18, 2013 at 1:18 PM, Edward A. Berry ber...@upstate.edu wrote:
In the mitocondrial inner membrane (which is very protein-dense) I believe
the most abundant protein is the adenine nucleotide transporter. (e.g.
Dear Crystallographers,
the Balbes webserver is now hosted at the Research Complex at Harwell,
on the Rutherford site. The new URL is
http://rcoisin.rc-harwell.ac.uk/BALBESSERV/
The service should still be considered somewhat experimental, due to
ongoing work to add another MR pipeline, MrBUMP,
Dear all
I have a somewhat philosophical question. Why do all protein sequences start
with a methionine (not referring to mature/processed form)? What is so special
about methionine and cannot be replaced by other amino acids?
Second, how does the ribosome know the first start codon is for
BLASPHEMY! haha
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Jacob
Keller
Sent: Monday, March 18, 2013 1:22 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Most Abundant Eukaryotic Membrane Protein List?
I don't want to crystallize the protein--I have another
Dear all,
As per the attached, we are really pleased to announce up to four positions to
join a structural biology team supporting drug discovery in the Northern
Institute for Cancer Research and the Chemistry Department, Newcastle
University. The structural biology positions, supported by
Dear Colleagues:
On behalf of the organizing committee of the International Conference on
Structural Genomics 2013 – Structural Life Science – (ICSG2013-SLS), we
cordially welcome you to the conference, to be held in Sapporo, Hokkaido,
Japan, July 29th – August 1st, 2013. ICSG2013-SLS is
I wouldn't be so sure that HeLa is just XX, or that it should be called
garden variety after what I read today.
http://www.nature.com/news/most-popular-human-cell-in-science-gets-sequenced-1.12609#/b1
-- David
On 18 March 2013 15:08, Jacob Keller j-kell...@fsm.northwestern.edu wrote:
Dear
Dear all,
I have used CNS to calculate the experimental phase of my structure.
After Heavy-atom search, Heavy-atom refinement/SAD phasing and SAD Phasing -
Density Modification - Selection of Map.
Some files outputted:
sad_phase2.hkl
sad_phase2.sdb
density_modify.hkl
density_modify.map
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