Marcelo Silva wrote:
The pdb command was: pdb2gmx -f prot.pdb -o prot_processed.gro -water spce
There is a total of 297 residues. The pdb2gmx indicates that there are
4573 atoms but the topology file indicates 4577 atoms.
It seems that is the arginine residue that is having problems:
172 opls_236 11 GLY O 56 -0.5 15.9994 ;
qtot 4
173 opls_238 12 ARG N 57 -0.5 14.0067 ;
qtot 3.5
174 opls_241 12 ARG H 57 0.3 1.008&nb!
! sp; ; qtot 3.8
175 opls_224B 12 ARG CA 57 0.14 12.011 ;
qtot 3.94
176 opls_140 12 ARG HA 57 0.06 1.008 ;
qtot 4
177 opls_136 12 ARG CB 58 -0.12 12.011 ;
qtot 3.88
178 opls_140 12 ARG HB1 58 0.06 1.008 ;
qtot 3.94
17! ! 9 opls_140 12 ARG HB2 58 0.06
1.008 ; qtot 4
180 opls_308 12 ARG CG 59 -0.05 12.011 ;
qtot 3.95
181 opls_140 12 ARG HG1 59 0.06 1.008 ;
qtot 4.01
182 opls_140 12 ARG HG2 59 -0.12 1.008 ;
qtot 3.89
More specifically, atom HG2 is having problems. It should be assigned a charge
of +0.06, not -0.12. The .rtp file distributed with Gromacs 4.5.3 is correct,
so I don't know how this is happening unless someone has messed with your .rtp
file. This difference of -0.18 accounts for the spurious charge.
-Justin
183 opls_307 &nbs! ! p; 12 ARG CD 60 0.19
12.011 ; qtot 4.08
184 opls_140 12 ARG HD1 60 0.06 1.008 ;
qtot 4.14
185 opls_140 12 ARG HD2 60 0.06 1.008 ;
qtot 4.2
186 opls_303 12 ARG NE 61 -0.7 14.0067 ;
qtot 3.5
187 opls_304 12 ARG ! ! ; HE 61 0.44
1.008 ; qtot 3.94
188 opls_302 12 ARG CZ 61 0.64 12.011 ;
qtot 4.58
189 opls_300 12 ARG NH1 62 -0.8 14.0067 ;
qtot 3.78
190 opls_301 12 ARG HH11 62 0.46 1.008 ;
qtot 4.24
191 opls_301 12 ARG HH12 62 &n! ! bsp; 0.46
1.008 ; qtot 4.7
192 opls_300 12 ARG NH2 63 -0.8 14.0067 ;
qtot 3.9
193 opls_301 12 ARG HH21 63 0.46 1.008 ;
qtot 4.36
194 opls_301 12 ARG HH22 63 0.46 1.008 ;
qtot 4.82
195 opls_235 12 ARG C 64 0.5 ! ! ;
12.011 ; qtot 5.32
196 opls_236 12 ARG O 64 -0.5 15.9994 ;
qtot 4.82
----------------------
725 opls_236 49 PRO O 237 -0.5 15.9994 ;
qtot 3.82
726 opls_238 50 ARG N 238 -0.5 14.0067 ;
qtot 3.32
727 opls_241 50 ARG H 238 0.3 &! ! nbsp;
1.008 ; qtot 3.62
728 opls_224B 50 ARG CA 238 0.14 12.011 ;
qtot 3.76
729 opls_140 50 ARG HA 238 0.06 1.008 ;
qtot 3.82
730 opls_136 50 ARG CB 239 -0.12 12.011 ;
qtot 3.7
731 opls_140 50 ARG HB1 239 0.06 1.008 ;
qtot 3.76
! ! 732 opls_140 50 ARG HB2 239 0.06
1.008 ; qtot 3.82
733 opls_308 50 ARG CG 240 -0.05 12.011 ;
qtot 3.77
734 opls_140 50 ARG HG1 240 0.06 1.008 ;
qtot 3.83
735 opls_140 50 ARG HG2 240 -0.12 1.008 ;
qtot 3.71
736 opls_307 ! ! 50 ARG CD 241 0.19 12.011
; qtot 3.9
737 opls_140 50 ARG HD1 241 0.06 1.008 ;
qtot 3.96
738 opls_140 50 ARG HD2 241 0.06 1.008 ;
qtot 4.02
739 opls_303 50 ARG NE 242 -0.7 14.0067 ;
qtot 3.32
740 opls_304 50 ARG HE ! ! ; 242 0.44
1.008 ; qtot 3.76
741 opls_302 50 ARG CZ 242 0.64 12.011 ;
qtot 4.4
742 opls_300 50 ARG NH1 243 -0.8 14.0067 ;
qtot 3.6
743 opls_301 50 ARG HH11 243 0.46 1.008 ;
qtot 4.06
744 opls_301 50 ARG HH12 243 0.46 &nb! ! sp;
1.008 ; qtot 4.52
745 opls_300 50 ARG NH2 244 -0.8 14.0067 ;
qtot 3.72
746 opls_301 50 ARG HH21 244 0.46 1.008 ;
qtot 4.18
747 opls_301 50 ARG HH22 244 0.46 1.008 ;
qtot 4.64
748 opls_235 50 ARG C 245 0.5 12.011 ;
qtot 5.14
! ! 749 opls_236 50 ARG O 245 -0.5 15.9994
; qtot 4.64
> Date: Mon, 7 Mar 2011 09:44:53 -0500
> From: [email protected]
> To: [email protected]
> Subject: Re: [gmx-users] # Protein non-integer charge
>
>
>
> Marcelo Silva wrote:
> > Thank you Mark and Justin,
> >
> > I didn't specified the termini, but when I choose the zwitterionic
forms
> > the net charge becomes -4.670.
> >
>
> You shouldn't; as I said before, zwitterionic termini are only for
single amino
> acids, not full-length proteins.
>
> > Without specifying the termini, the first non integer residue is
residue
> > nr. 12 arginine: qtot 4 to qtot 4.82.
>
> Are you missing any atoms? What was ! ! your exact pdb2gmx command?
>
> -Justin
>
> > If both termini are in the zwitterionic forms, the error is right
at the
> > 1st residue (methionine): total charge: 0.9
> >
> > > Date: Mon, 7 Mar 2011 09:21:08 -0500
> > > From: [email protected]
> > > To: [email protected]
> > > Subject: Re: [gmx-users] # Protein non-integer charge
> > >
> > >
> > >
> > > Marcelo Silva wrote:
> > > > Hi everybody,
> > > >
> > > > My problem is the following: I am studying the chromosome
partitioning
> > > > protein ParB from Burkholderia cenocepacia J2315. As no crystal
> > > > structure was available, I used I-TASSER to predict its 3d
structure.
> > > >
> > > > In order to refine the structure, I am now using in Gromacs the
pdb > > f! ! ile
> > > > I've obtained, following the Lysozime tutorial:
> > > >
> >
http://www.bevanlab.biochem.vt.edu/Pages/Personal/justin/gmx-tutorials/lysozyme/index.html.
> > > >
> > > > The problem is that after running pdb2gmx the protein has a net
charge
> > > > of -4.68, which indicates that a problem has ocurred, but pdb2gmx
> > > > doesn't seem to be presenting any critical error message.
> > > >
> > >
> > > This usually happens when you've chosen termini incorrectly. The
> > tutorial
> > > doesn't require you to select termini, since the defaults (NH3+ and
> > COO-) are
> > > correct. Are you choosing something else? Usually with OPLS the
> > problem is
> > > choosing zwitterionic termini when not dealing with a single amino
> > acid, whi! ! ch
> > > is the only time these termini are appropriate.
> > >
> > > -Justin
> > >
> > > > PDB file:
http://zhanglab.ccmb.med.umich.edu/I-TASSER/output/S64445/
> > > >
> > > > Be! ! st regards,
> > > >
> > > > Marcelo
> > > >
> > > >
> >
------------------------------------------------------------------------
> > > >
> > > > pdb2gmx output:
> > > >
> > > > Opening library file /usr/share/gromacs/top/ffoplsaa.rtp
> > > > Opening library file /usr/share/gromacs/top/aminoacids.dat
> > > > Opening library file /usr/share/gromacs/top/aminoacids.dat
> > > > WARNING: masses will be determined based on residue and atom names,
> > > > this can deviate from the real mass of the atom type> > > >
Opening library file /usr/share/gromacs/top/atommass.dat
> > > > Entries in atommass.dat: 178
> > > > WARNING: vdwradii will be determined based on residue and atom
names,
> > > > this can deviate from the real mass of the atom type
> > > > Opening library file /usr/share/gromacs/top/vdwradii.dat
> > > > Entries in vdwradii.dat: 28< br>Opening library file
> > &! ! gt; > /usr/share/gromacs/top/dgsolv.dat
> > > > Entries in dgsolv.dat: 7
> > > > Opening library file /usr/share/gromacs/top/electroneg.dat
> > > > Entries in electroneg.dat: 71
> > > > Opening library file /usr/share/gromacs/top/elements.dat
> > > > Entries in elements.dat: 218
> > > > Reading prot.pdb...
> > > > Read 'protein', 4573 atoms
> > > > Opening library file! ! /usr/share/gromacs/top/xlateat.dat
> > > > 26 out of 26 lines of xlateat.dat converted succesfully
> > > > Analyzing pdb file
> > > > There are 1 chains and 0 blocks of water and 297 residues with
4573
> > atoms
> > > >
> > > > chain #res #atoms
> > > > 1 'A' 297 4573
> > > >
> > > > All occupancies are one
> > > > Opening library file /usr/share/gromacs/top/ffoplsaa.atp
> > > > Atomtype 1
> > > > Reading residue database... (ffoplsaa)
> > > > Opening library file /usr/share/gromacs/top/ffoplsaa.rtp
> > ! ! > > Residue 59
> > > > Sorting it all out...
> > > > Opening library file /usr/share/gromacs/top/ffoplsaa.hdb
> > > > Opening library file /usr/share/gromacs/top /ffoplsaa-n.tdb
> > > > Opening li! ! brary file /usr/share/gromacs/top/ffoplsaa-c.tdb
> > > >
> > > > Back Off! I just backed up topol.top to ./#topol.top.7#
> > > > Processing chain 1 'A' (4573 atoms, 297 residues)
> > > > There are 451 donors and 430 acceptors
> > > > There are 670 hydrogen bonds
> > > > Will use HISB for residue 137
> > > > Will use HISB for residue 150
> > > > Will use HISB for residue 190
> > > > Will use HISB for residue 207
> > > > Will use HISB for residue 225
> > > > Checking for duplicate atoms....
> > > > Opening library file /usr/share/gromacs/top/specbond.dat
> > > > 7 out of 7 lines of specbond.dat converted succesfully
> > > > Special Atom Distance matrix:
> > > > MET1 ! ! MET53 MET71 MET119 HISB137 HISB150 MET180
> > > > SD10 SD7! ! 95 SD1051 SD1801 N E22091 NE22301 SD2752
> > > > MET53 SD795 2.734
> > > > MET71 SD1051 3.599 1.900
> > > > MET119 SD1801 3.866 2.738 1.752
> > > > HISB137 NE22091 3.420 2.337 2.726 1.784
> > > > HISB150 NE22301 3.300 3.399 3.547 2.251 1.488
> > > > MET180 SD2752 2.714 2.430 3.872 3.588 2.019 2.534
> > > > MET188 SD2867 1.831 2.554 3.389 2.903 1.893 1.645 1.520
> > > > HISB190 NE22894 1.854 2.621 3.979 3.803 2.535 2.621 1.015
> > > > HISB207 NE23144 3.293 3.005 4.536 4.229 2.555 3.052 0.734
> > > > MET214 SD3267 2.343 3.284 4.746 4.546 3.162 3.163 1.349
> > > > HISB225 NE23449 3.197 4.310 5.713 5.308 3.829 3.582 2.113
> > > > MET188 HISB190 HISB207 MET214
> > > > ! ! SD2867 NE22894 NE23144 SD3267
> > > > HISB190 NE22894 1.112
> > > > HISB207! ! NE23144 2.169 1.485
> > > > MET214 SD3267 1.790 0.783 1.422
> > > > HISB225 NE23449 2.522 1.762 1.900 1.063
> > > > N-terminus: NH3+
> > > > C-terminus: COO-
> > > > Now there are 297 residues with 4577 atoms
> > > > Making bonds...
> > > > Opening library file /usr/share/gromacs/top/aminoacids.dat
> > > > Number of bonds was 4596, now 4596
> > > > Generating angles, dihedrals and pairs...
> > > > Before cleaning: 12035 pairs
> > > > Before cleaning: 12105 dihedrals
> > > > Keeping all generated dihedrals
> > > > There are 12105 dihedrals, 838 impropers, 8351 angles
> > > > 12017 pairs, 4596 bonds and 0 virtual sites
> > > > Total mass 32038.885 a.m.u.
> > > > Total charge -4.680 e
> > > > Writing topology> > > >
> > > > Back Off! I just! ! backed up posre.itp to ./#posre.itp.4#
> > > >
> > > > Writing coordinate file...
> > > >
> > > > Back Off! I just backed up prot_processed.gro to
> > ./#prot_processed.gro.4#
> > > > --------- PLEASE NOTE ------------
> > > > You have succesfully generated a topology from: prot.pdb.
> > > > The oplsaa force field and the spce water model are used.
> > > > Note that the default mechanism for selecting a force fields has
> > > > changed, starting from GROMACS version 3.2.0
> > > > --------- ETON ESAELP ------------
> > > >
> > >
> > > --
> > > ========================================
> > >
> > > Justin A. Lemkul
> > > Ph.D. Candidate
> > > I! ! CTAS Doctoral Scholar
> > > MILES-IGERT Trainee
> > > Department of Biochemistry
> > > Virginia Tech
> > > Blacksburg, VA
> > > jalemkul[at]vt.edu | (540) 231-9080
> > > http://www.bevanlab.biochem.vt.edu/Pages/Personal/justin
> > >
> > >! ! ========================================
> > > --
> > > gmx-users mailing list [email protected]
> > > http://lists.gromacs.org/mailman/listinfo/gmx-users
> > > Please search the archive at
> > http://www.gromacs.org/Support/Mailing_Lists/Search before posting!
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> > > www interface or send it to [email protected].
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>
> --
> ========================================
>! !
> Justin A. Lemkul
> Ph.D. Candidate
> ICTAS Doctoral Scholar
> MILES-IGERT Trainee
> Department of Biochemistry
> Virginia Tech
> Blacksburg, VA
> jalemkul[at]vt.edu | (540) 231-9080
> http://www.bevanlab.biochem.vt.edu/Pages/Personal/justin
>
> ========================================
> --
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--
========================================
Justin A. Lemkul
Ph.D. Candidate
ICTAS Doctoral Scholar
MILES-IGERT Trainee
Department of Biochemistry
Virginia Tech
Blacksburg, VA
jalemkul[at]vt.edu | (540) 231-9080
http://www.bevanlab.biochem.vt.edu/Pages/Personal/justin
========================================
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