[gmx-users] adding new atoms in .itp file

Viswanadham Sridhara muta.mestri at gmail.com
Thu Dec 22 20:08:57 CET 2005


Hi David,
I did with -inter option and it worked, now I got the itp file for protein.
And I have taken dppc bilayer from Dr.Tieleman's website, and I inserted
protein in bilayer.
Now my question is, should my topology file look like this:
#include "ffgmx.itp"
#include "protein.itp"
#include "dppc.itp".......and so on.
I got an error while running energy minimisation,
it ended saying fmax norm is infinity on one atom, should I do any other
steps in between, am using flexible water for EM.
Thanks in advance,
Vissu


On 12/21/05, David van der Spoel <spoel at xray.bmc.uu.se> wrote:
>
> Viswanadham Sridhara wrote:
>
> > The only problem with my pdb file is that it has 1330 atoms, I think I
> > cant use prodrg with more than 300.......
> > As you pointed out, I will try to make a decent pdb file.
> >
> > One more question,
> > This is a part of my .itp file
> >
> > 295          N     40    GLU      N    206      -0.28    14.0067   ;
> > qtot -1.28
> >    296          H     40    GLU      H    206       0.28      1.008
> > ; qtot -1
> >    297        CH1     40    GLU     CA    207          0     13.019
> > ; qtot -1
> >    298        CH2     40    GLU     CB    208          0     14.027
> > ; qtot -1
> >    299        CH2     40    GLU     CG    209          0     14.027
> > ; qtot -1
> >    300          C     40    GLU     CD    210       0.27     12.011
> > ; qtot -0.73
> >    301         OM     40    GLU    OE1    210     -0.635    15.9994
> > ; qtot -1.365
> >    302         OM     40    GLU    OE2    210     -0.635    15.9994
> > ; qtot -2
> >    303          C     40    GLU      C    211       0.38     12.011
> > ; qtot -1.62
> >    304          O     40    GLU      O    211      -0.38    15.9994
> > ; qtot -2
> >
> > while in pdb file,
> >
> > ATOM    295  N   GLU    40      20.250  25.090  41.950  1.00  0.00
> > ATOM    296  H   GLU    40      20.340  25.930  41.420  1.00  0.00
> > ATOM    297  CA  GLU    40      20.620  25.440  43.320  1.00  0.00
> > ATOM    298  CB  GLU    40      21.210  26.840  43.440  1.00  0.00
> > ATOM    299  CG  GLU    40      22.630  26.980  42.910  1.00  0.00
> > ATOM    300  CD  GLU    40      23.050  28.450  42.940  1.00  0.00
> > ATOM    301  OE1 GLU    40      22.680  29.310  42.130  1.00  0.00
> > ATOM    302  OE2 GLU    40      23.780  28.750  44.050  1.00  0.00
> > ATOM    303  HE2 GLU    40      24.010  29.710  43.890  1.00  0.00
> > ATOM    304  C   GLU    40      19.560  25.240  44.400  1.00  0.00
> > ATOM    305  O   GLU    40      19.800  24.810  45.530  1.00  0.00
> >
> > if you can see, HE2 is missing in .itp file, when i used pdb2gmx
> > program, this might be due to its description in ffgmx.rtp file which is
> > [ GLU ]
> >  [ atoms ]
> >      N     N  -0.280     0
> >      H     H   0.280     0
> >     CA   CH1   0.000     1
> >     CB   CH2   0.000     2
> >     CG   CH2   0.000     3
> >     CD     C   0.270     4
> >    OE1    OM  -0.635     4
> >    OE2    OM  -0.635     4
> >      C     C   0.380     5
> >      O     O  -0.380     5
> >
> > %%%%%%%%%%%
> > Should I add that atom type in .rtp file, or is there any other way
> > pdb2gmx can take care of this.
>
>
> No, you should run pdb2gmx -inter and select GLUH for the residue in
> question. This will put the proton on OE1, but that should still give
> the same effect.
>
> > Thanks in advance,
> > Vissu
> >
> >
> > On 12/21/05, *David van der Spoel* <spoel at xray.bmc.uu.se
> > <mailto:spoel at xray.bmc.uu.se>> wrote:
> >
> >     Viswanadham Sridhara wrote:
> >
> >     >
> >     > Hi Everyone,
> >     > I have a .itp file, where I want to add new atoms in between, is
> >     there
> >     > any way that I can add them at the end, but give the respective
> >     > residue number, or should they be in order and represent .pdb
> file.
> >
> >
> >     Not easy (ch. 5). Try other means, maybe prodrg, or make a good
> >     pdb file
> >     from it (if it is a protein).
> >
> >     > Thanks,
> >     > -Vissu
> >     > --
> >     >
> >
> >------------------------------------------------------------------------
> >
> >     >
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> >
> >     --
> >     David.
> >
> ________________________________________________________________________
> >     David van der Spoel, PhD, Assoc. Prof., Molecular Biophysics group,
> >     Dept. of Cell and Molecular Biology, Uppsala University.
> >     Husargatan 3, Box 596,          75124 Uppsala, Sweden
> >     phone:  46 18 471 4205          fax: 46 18 511 755
> >     spoel at xray.bmc.uu.se
> >     <mailto:spoel at xray.bmc.uu.se>    spoel at gromacs.org
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> >
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> >
> > --
> > Viswanadham Sridhara,
> > Graduate Research Assistant,
> > Old Dominion University, "VIRGINIA".
> >
> >------------------------------------------------------------------------
> >
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> --
> David.
> ________________________________________________________________________
> David van der Spoel, PhD, Assoc. Prof., Molecular Biophysics group,
> Dept. of Cell and Molecular Biology, Uppsala University.
> Husargatan 3, Box 596,          75124 Uppsala, Sweden
> phone:  46 18 471 4205          fax: 46 18 511 755
> spoel at xray.bmc.uu.se    spoel at gromacs.org   http://xray.bmc.uu.se/~spoel
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--
Viswanadham Sridhara,
Graduate Research Assistant,
Old Dominion University, "VIRGINIA".
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