From: Brian Bennion (brian_at_youkai.llnl.gov)
Date: Thu Apr 29 2004 - 13:23:55 CDT
What happens if you just leave out the first and last directives in your
psfgen script?
Brian
On Thu, 29 Apr 2004, Edward Patrick Obrien wrote:
>
> I tried sending this message yesterday but it appears it didn't go
> through...
>
> On Wed, 28 Apr 2004, Ed wrote:
>
>  Hi All,
>     Serious problem here (I think), I create a .pdb and .psf with patches
>  of CT3 (methyl amide) and ACE, but in the .psf file there is no angle
>  definitions nor dihedral definitions for the patched atoms!
>
>     This leads to serious problems... when I minimize, or run MD, the atoms
>  in the patches contort and float around like they don't feel each other,
>  outrageous bond angles can occur! And finally the system crashes at some
>  point because RATTLE can't take it.
>
>     Why are angle and dihedral not being defined? How can I correct it?
>
>     Just in case you don't believe me check this out:
>
>     If I just use the Standard NTER and CTER in charmm (less atoms then ACE
>  and CT3) the number of angles and dihedrals are:
>
>  	Info: writing psf file test.psf
>  	total of 172 atoms
>  	total of 174 bonds
>  	total of 314 angles
>  	total of 461 dihedrals
>  	total of 21 impropers
>
>     Now if I patch with CT3 and ACE:
>
>          Info: writing psf file test.psf
>          total of 181 atoms
>          total of 183 bonds
>          total of 307 angles
>          total of 453 dihedrals
>          total of 24 impropers
>
>     So there are more Atoms but less angles and dihedrals? Sounds crazy to
>  me.
>
>     Also here are the positions of the hydrogens on the carbon of the
>  amide-methyl BEFORE minimization:
>
>  ATOM    170  HT1 SER    11      19.167  -0.569   0.788  1.00  0.00
>  ATOM    171  HT2 SER    11      19.311  -2.153   1.177  1.00  0.00
>  ATOM    172  HT3 SER    11      20.181  -1.533  -0.064  1.00  0.00
>
>     Here are the same hydrogens AFTER 2000 steps of minimization:
>
>  ATOM    170  HT1 SER    11      20.509  -1.046   0.825  1.00  0.00
>  ATOM    171  HT2 SER    11      20.560  -1.180   0.961  1.00  0.00
>  ATOM    172  HT3 SER    11      20.432  -1.047   0.906  1.00  0.00
>
>     Notice anything strange!? The atoms are practically on top of each
>  other!?
>
>     Here is the TCL script I use to create the .pdb and .psf:
>
>  package require psfgen
>  topology top_all27_prot_lipid.inp
>          segment X {
>          first none
>          last none
>          pdb X_start.pdb}
>          patch ACE X:1
>          patch CT3 X:11
>          coordpdb X_start.pdb X
>          guesscoord
>          writepdb test.pdb
>          writepsf test.psf
>
>  Any suggestions would be much appreciated,
>  Ed
>
>  PS - I've tried using 'auto' to no avail.
> >
> >
>
*****************************************************************
**Brian Bennion, Ph.D.                                         **
**Computational and Systems Biology Division                   **
**Biology and Biotechnology Research Program                   **
**Lawrence Livermore National Laboratory                       **
**P.O. Box 808, L-448    bennion1_at_llnl.gov                     **
**7000 East Avenue       phone: (925) 422-5722                 **
**Livermore, CA  94550   fax:   (925) 424-6605                 **
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