Dear All,
I am able to do the superposition of the ligand with suplig.f program and
superpose also do the same.
Thank you for your valuable suggestions.
regardsvijay
Vijay
On Tuesday, 26 May 2015 6:11 PM, vijay srivastava
wrote:
Dear All,
I want to superpose the nucleotide form
Dear All,
I want to superpose the nucleotide form one GTPase on to the nucleotide of
other GTPase in order to study
the interaction in the nucleotide binding pocket. I tried to superpose but it
is superposing on the basis of secondary structure as aresult both the
nucleotides from two structutr
Dear All,
Sorry to disturb you all it can be easily done in ccp4mg.
regards Vijay
On Saturday, 9 May 2015 4:36 PM, vijay srivastava
wrote:
Dear All,
In coot is there is any option so that we can change the colour of atoms. As in
ball and stick model in default
it is showing
Dear All,
In coot is there is any option so that we can change the colour of atoms. As in
ball and stick model in default
it is showing sulphur as green.
could we change the colour of atoms to show carbon in gray, oxygen in red and
suphur in yellow.
regards Vijay
Dear Dr. Sacha,
it is giving following error after typing the command
global: Command not found.
wm: Command not found.
set: Variable name must begin with a letter.
Vijay
On Thursday, 24 July 2014 4:21 PM, Raghurama P Hegde
wrote:
Hi Sanjit,
These two reviews throw some light o
Dear All,
Is there is any program to convert euler angles into theta, phi and kappa?
regards
Vijay
great for finding the sites, but at this
resolution you want to refine the sites, and calculate phases with other
programs/pipelines, like Phaser/Crank/Crunch.
best,
Kay
On Tue, 3 Jun 2014 16:37:58 +0800, vijay srivastava
wrote:
>Dear All,
Does anyone know of a facility
that provides amino a
Hi,
I am trying to clone a 1.2kb insert into a expression vector pET 23a through
T/A cloning. The restriction enzyme used is Nhe1(NEB) and BamH1 (NEB) in the
forward and reverse primer recpectively. I was succesful in subcloning (T/A
vector) and getting my insert at 1.2kb after double digesti
hi
i am facing problem in cloning,getting my insert and vector at the
correct position after digestion but after ligation colony is not
coming and if how it is coming than i am not getting my insert
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