Which papers have you read so far?
Catch ya,
Dr. Dallas Warren
Drug Discovery Biology
Monash Institute of Pharmaceutical Sciences, Monash University
381 Royal Parade, Parkville VIC 3052
dallas.war...@monash.edu
+61 3 9903 9304
-
When the only tool you own is a hamm
On 7/14/13 9:03 PM, Rama wrote:
Hi,
How to get a snapshots in equal intervals of time (250ps) from production MD
trajectory. I'm using -sep , -t0, -timestep but output came only one .gro
file.
trjconv -skip -sep should work, but without exact command lines and the output
you received (as w
Hi,
How to get a snapshots in equal intervals of time (250ps) from production MD
trajectory. I'm using -sep , -t0, -timestep but output came only one .gro
file.
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any one please help me out with this problem?
2013/7/10 Ahmet yıldırım
> Dear users,
>
> I extracted separate extreme projections using g_anaeig. I have to make
> pictures which show the difference. Can you help me, someone who makesthem
> using pymolbefore
> ?
>
> --
> Ahmet Yıldırım
>
--
Can anybody help me understand these better?
2013/7/10 lloyd riggs
> There vectors. Theres some good older papers explaining the whole thing
> from Van Gunstern, Berendsen, and some other good ones from de Groot that
> explain them well and includes combining them with other data analysis
> ty
On 7/14/13 7:07 PM, jriedel wrote:
Hi,
I'm want to run a MD simulation with a Phe-Phe-Phe-Phe-Gly cyclic peptide.
But I'm have problems generating the topology files. When I try to use the
strategy to generate a topology file for the linear GF
using
pdb2gmx -ff charmm27 -f pep.pdb -o pep.g
Hi,
I'm want to run a MD simulation with a Phe-Phe-Phe-Phe-Gly cyclic peptide.
But I'm have problems generating the topology files. When I try to use the
strategy to generate a topology file for the linear GF
using
pdb2gmx -ff charmm27 -f pep.pdb -o pep.gro -ter -water spce
and choosing None f
On 7/14/13 2:23 PM, fatemeh ramezani wrote:
Hello dear users
I'm simulating gold nanoparticle interaction with protein. I want to change the
pH of system. What would need to be changed to simulate this system at pH 3.0?
As is discussed frequently on this list (hint: check the archive for
Hello dear users
I'm simulating gold nanoparticle interaction with protein. I want to change the
pH of system. What would need to be changed to simulate this system at pH 3.0?
thanks you
Fatemeh Ramezani
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Error message, аfter the make:
In file included from
/cygdrive/d/1/gromacs-4.6.3/src/gmxlib/thread_mpi/atomic.c:38:0:
/cygdrive/d/1/gromacs-4.6.3/src/gmxlib/thread_mpi/impl.h:504:20: ошибка:
field «timer_init» has incomplete type
src/gmxlib/CMakeFiles/gmx.dir/build.make:8061: recipe for target
`sr
On 7/14/13 1:04 PM, bh...@udsu.ru wrote:
Hello,
How to compile Cygwin 4.6.3 for Windows using Cygwin ?
I did so:
tar xfz gromacs-4.6.tar.gz
cd gromacs-4.6
The version 4.6 tarball will not give you version 4.6.3 :) Unless this is a
typo, make sure you're actually working with the newest
On 7/14/13 11:36 AM, Nilesh Dhumal wrote:
Hello,
I am trying to run the qm-mm gas phase calculations for my system.
I am using following in md.mdp file.
title = cpeptide MD
cpp = /usr/bin/cpp
integrator = md
dt = 0.001; ps !
ns
Hello,
How to compile Cygwin 4.6.3 for Windows using Cygwin ?
I did so:
tar xfz gromacs-4.6.tar.gz
cd gromacs-4.6
mkdir build
cd build
cmake .. -DGMX_BUILD_OWN_FFTW=ON
(fftw 3.3 - install)
make
Error message
Thank you.
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Hello,
I am trying to run the qm-mm gas phase calculations for my system.
I am using following in md.mdp file.
title = cpeptide MD
cpp = /usr/bin/cpp
integrator = md
dt = 0.001; ps !
nsteps = 500 ; total 5 ps.
On 7/14/13 6:21 AM, Albert wrote:
Hello:
I've got a question on energygrps options in .mdp file. This option is usually
used for establishing the groups for the energy output. I am going to study the
entropy changes of protein-ligand-SOL in a membrane system, I am just wondering
shall I spe
Hi all,
Just a quick question - and perhaps some wisdom from those with more experience.
I am trying to use metadynamics with gromacs to plot an energy landscape about
the rotation of two proteins. If I were to define my collective variables as
ThetaA and ThetaB, Theta being the rotation about
Hello:
I've got a question on energygrps options in .mdp file. This option is
usually used for establishing the groups for the energy output. I am
going to study the entropy changes of protein-ligand-SOL in a membrane
system, I am just wondering shall I specify each compoenent in
energygrps
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