QUICK ERRATUM
Sorry W, I forgot a very important bit (I was half asleep ;-)). As the unit
cells are, it would not be correct to import one set of Rfree flags from one
dataset to the other in sftools as the axes are moved around and the indexing
is no longer consistent between the two mtzs.
CAVEAT
The procedure discussed in previous email to try to simply import one set of
Rfree flags from on mtz to the other, however, would required a very carefully
choice of matching unit cells origins ...
This problem would be overcome by expanding the orthorombic lattice to the
primitive
I introduce myself as Dr.Krithika Gokulnath, CAS in crystallography and
Biophysics, UNiversity of Madras. I have been working with a cloned protein and
have been successfully able to crystallise it. However data collection done at
home source shows a pattern of streaks instead of spots. The
Dear Krithika,
what you probably see is the diffraction pattern of a highly mosaic
crystal due to probably internal disordering.
cheers
Demetres
On 3/10/2013 3:40 μμ, Krithika GOkulnath wrote:
I introduce myself as Dr.Krithika Gokulnath, CAS in crystallography and
Biophysics, UNiversity
Lipid or PEG from your crystallisation condition?
---
Dr Antony W Oliver
Senior Research Fellow
CR-UK DNA Repair Enzymes Group
Genome Damage and Stability Centre
Science Park Road
University of Sussex
Falmer, Brighton, BN1 9RQ
email: antony.oli...@sussex.ac.uk
tel (office): +44 (0)1273 678349
Dear Andre,
It always impressive to see a near atomic resolution structure with a bound
lipid. Congratulations. However, to identify what lipid you have requires a
bit more analysis than just looking in databases. First, what is the bacterium
you are using as the host? If it is E. coli,
Dear Michael, thank you for the prompt reply.
The host was indeed E. coli.
From what I have been reading I completely agree on the lack of biological
support for such a molecule but still the map seems very convincing of the
presence of cis bonds at such positions... Could such a conformation
When USA budget is back :-\ you may give a try to :
http://webbook.nist.gov/chemistry/
It helped me several times, very intuitive, I use just a formula for a search,
it also accept a wild character for unknown number of atoms.
FF
Dr Felix Frolow
Professor of Structural Biology and
Hi Chris,
Though there is no alternative to have a co-crystal structure it does not
always happened to be the ideal case where you would easily get it
co-crystallized in the same condition.
Soaking worked well in many cases, though definitely the answer is very
dependent on a particular case to
One standard thing to do would be to set up a grid around the condition and
then try picking crystals from different well to see if any of them produce
better looking diffraction patterns. If that does not work one might give
any of the commercially available additive screen a try to see if
Hi all,
Sorry for the non-CCP4 question. I am looking for a type I transmembrane
protein in yeast, which resides on the plasma membrane instead of ER or Golgi.
A quick search in the database returns a large number of transmembrane proteins
with multiple TMs or targeted to various compartments.
==
Beamtime available at CHESS, October 16 - December 13, 2013
==
The CHESS/MacCHESS facility, located at Cornell University in Ithaca,
NY, invites macromolecular
Yes, and the mosaicity might have been poor to start with, or it might have
been caused by sub-optimal freezing conditions, assuming that the crystal was
frozen (not enough information to tell). I recommend doing a room temperature
diffraction experiment to see which it is and act accordingly -
Depends a bit on what the streaks look like. If they are curved, and
your streaks are connecting partial rings at different resolutions,
then what you may be seeing is simply diffuse scatter from a small
molecule, such as ice. The only way to be sure you are looking at
protein is if you see
Hi Bernhard,
I manage our websites (including 'c6.csiro.au') and have some experience of
your situation, as earlier this year we upgraded our server from IIS 6.0 - IIS
8.0
I don't know the full details of what your setup is, (e.g. I am assuming you
have full access to the machine, it is not
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