Hi CCP4ers
firstly apologies that this is slighty off ccp4 topic but does anyone know of a
programme whereby I can use solvent flipping with multi domain masks in
addition to a solvent mask for my phases i.e. not based on a model? I
wanted to use CNS density_modify (my maps are currently from
Raji
aside from the possibilites of toxic protein as already mentioned..
we had great results with overnight induction at 20oC for a protein that was
somewhat insoluble at 37oC. One thing that might work for you is to grow the
cells to OD 0.5 then lower the temperature to say 18 or 20.
Hi there
I quite like the Amicon stirred ultra concentration cell systems. You
can put large volumes in, maximum 1 litre size, I think. As well you
can attach an inert gas such as Argon or Nitrogen, for the gaseous
pressure, this reduces oxidation of your sample while it
concentrates.
Dear CCP4ers
can anyone recommend papers describing crystal structures of proteins
with a large functionally important disordered domain or domains.
Thanks in advance
Gina
and Associate Consultant II
Mayo Clinic Cancer Center
Griffin Cancer Research Building, Rm 310
4500 San Pablo Road
Jacksonville, FL 32224
(904) 953-6372 (office)
(904) 953-0046 (lab)
-Original Message-
From: CCP4 bulletin board [mailto:[EMAIL PROTECTED] On Behalf Of
Gina Clayton
Sent: Friday
Hi CCP4ers
Apologies for the off topic...
I have been trying to get hold of L-ribulose-5-phosphate (D- is readily
available). Does anyone know where I can get such a compound?
Thanks in advance for any suggestions and Merry Xmas!
Gina
There is also another paper on this that may be useful...
Acta Cryst. (2005). D61, 67-74.
Correction of X-ray intensities from single crystals containing
lattice-translocation defects. J Wang et al.
Regards
-Original Message-
From: CCP4 bulletin board [mailto:ccp...@jiscmail.ac.uk]
Posted on behalf of Professor John Hunt and Professor Liang Tong, North Eastern
Structural Genomics Consortium at Columbia University USA.
An accomplished and dynamic senior scientist is sought to join the
high-throughput protein biochemistry / crystallography group of the Northeast
Structural