On Sep 18 2007, Bryan W. Lepore wrote:
i wrote
(ensemble) / (sequence) to get a percent composition
i forgot to emphasize that i do not mean the Vm or the Z composition,
but the composition as one would enter e.g.
COMPosition ENSEmble mol1 FRACtional 0.22
or
COMPosition SCAttering
I cant answer - but this version certainly generates anisotropic scales..
We have ccp4.6.0.2 installed)
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unsubscibe
Go to the jiscmail page and follow the directions.
On Thu, 20 Sep 2007 16:31:07 +0200
Anat Bashan [EMAIL PROTECTED] wrote:
unsubscibe
On Thu, 20 Sep 2007 17:23:05 +0100
R. J. Lewis [EMAIL PROTECTED] wrote:
a large signalling complex called the 'stressosome' from B. subtilis.
-
If you decide to go for the human form of this signalling complex, I am an
over-producing strain.
You'd need quite a large French press or meat grinder to crack the cells
and get the protein.
William Scott wrote:
On Thu, 20 Sep 2007 17:23:05 +0100
R. J. Lewis [EMAIL PROTECTED] wrote:
a large signalling complex called the 'stressosome' from B. subtilis.
-
Hi,
apart from the ccp4 contact it's also worth checking the following
servers:
pisa:
http://www.ebi.ac.uk/msd-srv/prot_int/pistart.html
protein-protein interaction server:
http://www.biochem.ucl.ac.uk/bsm/PP/server/index.html
Cheers
Nikos
Xiaoyi Deng wrote:
Dear all:
I used moleman2 to
If you just want the residues involved in the interface, you can use the
byres selection commands in Pymol.
select contacts, (byres monA and (monB around 4))
which will show all the residues on monA that are within 4 Ang. of Mon
B.
Steve
-Original Message-
From: CCP4 bulletin board
Dear All,
I wanted to solve one of my new structures by molecular
replacement. I got three short search motifs from three
different structures available in the PDB. My question is, how
do I use all the search models to solve the structure.
With by best regards,
Sekar
(\_/)
(='.'=)
