This is an old version of the c++ libraries. You get it by installing
compat-libstdc++-33
Andreas
Paul Kraft wrote:
Hiys,
I've got an hp pavillion dv2000 with a 64x2 processor and I loaded the
redhat version of CCP4-6.0.2. I tried loading it manually but there was
no configure or make file
Coot has an expert mode which allows you to customise your FFT to some
extent - you will need to turn the fcf file into an mtz file, but that
is easy.. ( See reflection utilities)
And then you can use the great flexibility of the FFT routines to
generate a map to read into COOT.
Eleanor
d
Hi.
If you can use yum, try
yum install compat-libstdc++-33
If you want to know what kind of package is needed,
yum provides libstdc++.so.5
Shinya Fushinobu
On 2007/06/19, at 16:16, Andreas Forster wrote:
This is an old version of the c++ libraries. You get it by installing
compat-libst
Hi all,
a few days ago I sent a post in which I was asking if anybody knew a
program to automatically define the hydrophobic core of a protein,
given the pdb.
Unfortunately I got no answers, and indeed a more thorough googling
around revealed that such a program might not exist.
So it seems I
I dont know the answer but have you looked at the PISA site at the eBI -
there is extensive documentation addressing these sorts of questions.
http://www.ebi.ac.uk/msd-srv/prot_int/pistart.html
Eleanor
Sebastiano Pasqualato wrote:
Hi all,
a few days ago I sent a post in which I was asking if an
Sebastiano,
I can suggests one approach to finding core residues..
CCP4mg will calculate the total asa buried per residue and residues can be
selected by the criteria of their buried area. One way to define the protein
core would be to select residues with, say, <5.0A*2 asa. You can easily se
while evaluating it, you might want to check the importance of buried
residues by looking at how conserved they are in homologs.
tommi
Quoting Eleanor Dodson <[EMAIL PROTECTED]>:
> I dont know the answer but have you looked at the PISA site at the eBI -
>
> there is extensive documentation addr
Hi,
There exists a formal analytical way in doing this using the "survol"
command in BRUGEL package.
In short, this command define the accessible surface (external and
cavities) to the probe you choose and creates
separate masks (ensembles) of all atoms/residues that define these surfaces.
The
Hi all,
I am doing a survey on computer usage in crystallography. The questionnaire
can be found on the following web page:
http://www.bioscienceforum.com/survey.html
Its point-and-click, with 10 short questions, and should take under 2
minutes to complete. You are not requested to enter you
