Adding a Residue to a Force Field#
Adding a new residue#
If you have the need to introduce a new residue into an existing force field so that you can use pdb2gmx, or modify an existing one, there are several files you will need to modify. You must consult the Reference Manual for description of the required format. Follow these steps:
Add the residue to the rtp file for your chosen force field. You might be able to copy an existing residue, rename it and modify it suitably, or you may need to use an external topology generation tool and adapt the results to the rtp format.
If you need hydrogens to be able to be added to your residue, create an entry in the relevant hdb file.
If you are introducing new atom types, add them to the
If you require any new bonded types, add them to
Add your residue to
residuetypes.datwith the appropriate specification (Protein, DNA, Ion, etc).
If the residue involves special connectivity to other residues, update
Note that if all you are doing is simulating some weird ligand in water, or some weird ligand
with a normal protein, then the above is more work than generating a standalone itp
file containing a
[moleculetype] (for example, by modifying the top produced by some
parameterization server), and inserting an
#include of that itp file into a top
generated for the system without that weird ligand.
Modifying a force field#
Modifying a force field is best done by making a full copy of the installed forcefield directory and
residuetypes.dat into your local working directory:
cp -r $GMXLIB/residuetypes.dat $GMXLIB/amber99sb.ff .
Then, modify those local copies as above. pdb2gmx will then find both the original
and modified version and you can choose the modified version interactively from the list, or if
you use the pdb2gmx
-ff option the local version will override the system version.
When using solvate to generate a box of solvent, you
need to supply a pre-equilibrated box of a suitable solvent for solvate
to stack around your solute(s), and then to truncate to give the simulation volume you desire. When
using any 3-point model (e.g.
TIP3P) you should specify
which will take this file from
the gromacs/share/top directory. Other water models (e.g.
TIP5P) are available as well. Check the contents of the
of your GROMACS installation. After solvation, you should then be sure to equilibrate for at
least 5-10ps at the desired temperature. You will need to select the right water model in your
top file, either with the
-water flag to pdb2gmx, or by editing
your top file appropriately by hand.
Non water solvent#
It is possible to use solvents other than water in GROMACS. The only requirements are that you have a pre-equilibrated box of whatever solvent you need, and suitable parameters for this species in a simulation. One can then pass the solvent box to the -cs switch of solvate to accomplish solvation.
A series of about 150 different equilibrated liquids validated for use with GROMACS, and for the OPLS/AA and GAFF force fields, can be found at virtualchemistry.
Making a non-aqueous solvent box#
Choose a box density and box size. The size does not have to be that of your eventual simulation
box - a 1nm cube is probably fine. Generate a single molecule of the solvent. Work out how much
volume a single molecule would have in the box of your chosen density and size. Use editconf
to place a box of that size around your single molecule. Then use editconf to move the
molecule a little bit off center. Then use genconf
-rot to replicate that box into a large
one of the right size and density. Then equilibrate thoroughly to remove the residual ordering of
the molecules, using NVT and periodic boundary conditions. Now you have a box you can pass to
-cs, which will replicate it to fit the size of the actual simulation box.
A common question that new users have is how to create a system with mixed solvent (urea or DMSO at a given concentration in water, for example). The simplest procedure for accomplishing this task is as follows:
Determine the number of co-solvent molecules necessary, given the box dimensions of your system.
Generate a coordinate file of a single molecule of your co-solvent (i.e.,
-ci -nmoloptions of gmx insert-molecules to add the required number of co-solvent molecules to the box.
Making Disulfide Bonds#
The easiest way to do this is by using the mechanism implemented with the
file and pdb2gmx. You may find pdb2gmx
is useful. The sulfur atoms will need to be in the same unit that pdb2gmx
is converting to a
moleculetype, so invoking pdb2gmx
correctly may be required. See pdb2gmx
-h. This requires that the
two sulfur atoms be within a distance + tolerance (usually 10%) in order to be recognised
as a disulfide. If your sulfur atoms are not this close, then either you can
edit the contents of
specbond.datto allow the bond formation and do energy minimization very carefully to allow the bond to relax to a sensible length, or
run a preliminary EM or MD with a distance restraint (and no disulfide bond) between these sulfur atoms with a large force constant so that they approach within the existing
specbond.datrange to provide a suitable coordinate file for a second invocation of pdb2gmx.
Otherwise, editing your top file by hand is the only option.