Hi Christian
One guess would be one of the possible post translational
modifications seen for Lysine. acetylation or a triple methylation.
However propionylations and butyrylations have also been observed on
lysine.
It looks like you could build in waters, you may want to leave this
lysine
Biology Laboratory (www.embl.org). NCMM is located in brand
new laboratories in the University of Oslo and National Hospital
Biomedical Campus in the Oslo Research Park and Preclinical Medicine
buildings. A new Structural Biology laboratory at NCMM, headed by Dr.
J. Preben Morth has been
Hi Christian
There is nothing uncommon about your cell parameters, take extra care to get
the beam center right during indexing, a few pixels can make all the difference.
gl
Preben
On 03/08/2010, at 13.45, Christian Strube wrote:
> Hi everybody,
>
> indexing of recently collected data gave me u
use fasta
>my_amazing_protein
THISMESSAGESHOULDHAVEBEENSENTTOTHEPHENIXBB
;-)
Preben
On 03/08/2010, at 14.19, Md. Munan Shaik wrote:
> Hi everybody,
> I have a problem with Phenix autobuild. I want to input sequence file
> together with the pdb and mtz that I got from molecular replacement. Bu
hi
remember to reindex your data to P21212 in case you used Phaser to search all
alternative orthorhombic SG's and it found P22121
Preben
On 03/10/2010, at 04.56, Jack Russel wrote:
> Hi all,
>
> I have collected a data at 2.9 Å and the solved the structure using phaser .
> the space group c
the reindexing have no effect on the R-factor, I did indeed mean to remember to
transform the co-ordiantes according to the indexing :-)
On 04/10/2010, at 11.27, Ian Tickle wrote:
>
> On Sun, Oct 3, 2010 at 6:34 PM, J. Preben Morth wrote:
> hi
> remember to reindex your data to P2
leading to a less-internally-consistent data set at
> the peak. Does this argument hold water?
>
> Jacob Keller
J. Preben Morth, Ph.D
Group Leader
Membrane Transport Group
Nordic EMBL Partnership
Centre for Molecular Medicine Norway (NCMM)
University of Oslo
P.O.Box 1137 Blindern
0318 Oslo, Norwa
Dear Engin
I would also like to comment. I our recent structure determination of
the sodium pump (3.5 A) (see morth JP et al 2007) we did not have
experimental phasing to more than 6 A for the Ta6Br12 clusters and 7 A
for the Pt sites. Both with extensive multicrystal averaging and phase
Dear Martin
You can either add the cluster as a powder, just dip the tip of a
needle in the powder and gently approach the drop with the needle, the
Ta6Br12 crystals will spray itself onto the drop. Then you just wait
for the crystal to turn green, I usually marked the position where the
