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NAME

       pdb2gmx - converts pdb files to topology and coordinate files

       VERSION 4.0.1

SYNOPSIS

       pdb2gmx -f eiwit.pdb -o conf.gro -p topol.top -i posre.itp -n clean.ndx
       -q clean.pdb  -[no]h  -nice  int  -[no]merge  -ff  string  -water  enum
       -[no]inter   -[no]ss   -[no]ter  -[no]lys  -[no]arg  -[no]asp  -[no]glu
       -[no]gln  -[no]his  -angle   real   -dist   real   -[no]una   -[no]ignh
       -[no]missing    -[no]v    -posrefc   real   -vsite   enum   -[no]heavyh
       -[no]deuterate

DESCRIPTION

       This program  reads  a  pdb  file,  reads  some  database  files,  adds
       hydrogens  to  the  molecules  and  generates  coordinates  in  Gromacs
       (Gromos) format and a topology in  Gromacs  format.   These  files  can
       subsequently be processed to generate a run input file.

       The force fields in the distribution are currently:

       oplsaa OPLS-AA/L all-atom force field (2001 aminoacid dihedrals)

       G43b1  GROMOS96 43b1 Vacuum Forcefield

       G43a1  GROMOS96 43a1 Forcefield

       G43a2  GROMOS96 43a2 Forcefield (improved alkane dihedrals)

       G45a3  GROMOS96 45a3 Forcefield

       G53a5  GROMOS96 53a5 Forcefield

       G53a6  GROMOS96 53a6 Forcefield

       gmx    Gromacs Forcefield (a modified GROMOS87, see manual)

       encads Encad all-atom force field, using scaled-down vacuum charges

       encadv Encad all-atom force field, using full solvent charges

       The corresponding data files can be found in the library directory with
       names  like  ffXXXX.YYY.  Check  chapter  5  of  the  manual  for  more
       information  about file formats. By default the forcefield selection is
       interactive, but you can use the  -ff option  to  specify  one  of  the
       short  names  above  on  the command line instead. In that case pdb2gmx
       just looks for the corresponding file.

       Note that a pdb file is nothing more than a file format,  and  it  need
       not necessarily contain a protein structure. Every kind of molecule for
       which there is support in the database can be converted.  If  there  is
       no support in the database, you can add it yourself.

       The  program  has  limited  intelligence, it reads a number of database
       files, that allow it to make special bonds (Cys-Cys,  Heme-His,  etc.),
       if necessary this can be done manually. The program can prompt the user
       to select which kind of LYS, ASP, GLU, CYS or HIS  residue  she  wants.
       For  LYS  the  choice is between LYS (two protons on NZ) or LYSH (three
       protons,  default),  for  ASP  and  GLU   unprotonated   (default)   or
       protonated,  for  HIS  the  proton  can be either on ND1 (HISA), on NE2
       (HISB) or  on  both  (HISH).  By  default  these  selections  are  done
       automatically.  For  His,  this is based on an optimal hydrogen bonding
       conformation. Hydrogen bonds are defined based on  a  simple  geometric
       criterium,  specified  by the maximum hydrogen-donor-acceptor angle and
       donor-acceptor  distance,  which  are  set  by   -angle  and      -dist
       respectively.

       Option   -merge  will  ask if you want to merge consecutive chains into
       one molecule definition, this can be useful for connecting chains  with
       a disulfide brigde or intermolecular distance restraints.

       pdb2gmx will also check the occupancy field of the pdb file.  If any of
       the occupanccies are not one, indicating that the atom is not  resolved
       well  in  the  structure, a warning message is issued.  When a pdb file
       does not originate from an X-Ray structure determination all  occupancy
       fields  may  be  zero.  Either  way, it is up to the user to verify the
       correctness of the input data (read the article!).

       During processing the atoms will  be  reordered  according  to  Gromacs
       conventions.  With  -n an index file can be generated that contains one
       group reordered in the same way. This allows you to  convert  a  Gromos
       trajectory  and  coordinate  file  to  Gromos. There is one limitation:
       reordering is done after the hydrogens are stripped from the input  and
       before  new  hydrogens  are  added.  This means that you should not use
       -ignh.

       The  .gro and  .g96 file formats  do  not  support  chain  identifiers.
       Therefore  it is useful to enter a pdb file name at the  -o option when
       you want to convert a multichain pdb file.

       The option  -vsite removes hydrogen and fast improper dihedral motions.
       Angular  and  out-of-plane motions can be removed by changing hydrogens
       into virtual sites  and  fixing  angles,  which  fixes  their  position
       relative  to neighboring atoms. Additionally, all atoms in the aromatic
       rings of the standard amino acids (i.e. PHE, TRP, TYR and HIS)  can  be
       converted  into  virtual  sites,  elminating the fast improper dihedral
       fluctuations in these rings. Note that in this case all other  hydrogen
       atoms  are  also converted to virtual sites. The mass of all atoms that
       are converted into virtual sites, is added to the heavy atoms.

       Also slowing down of dihedral motion can be done with  -heavyh done  by
       increasing  the  hydrogen-mass  by a factor of 4. This is also done for
       water hydrogens to slow down  the  rotational  motion  of  water.   The
       increase in mass of the hydrogens is subtracted from the bonded (heavy)
       atom so that the total mass of the system remains the same.

FILES

       -f eiwit.pdb Input
        Structure file: gro g96 pdb tpr tpb tpa

       -o conf.gro Output
        Structure file: gro g96 pdb

       -p topol.top Output
        Topology file

       -i posre.itp Output
        Include file for topology

       -n clean.ndx Output, Opt.
        Index file

       -q clean.pdb Output, Opt.
        Structure file: gro g96 pdb

OTHER OPTIONS

       -[no]hno
        Print help info and quit

       -nice int 0
        Set the nicelevel

       -[no]mergeno
        Merge chains into one molecule definition

       -ff string select
        Force field, interactive by default. Use -h for information.

       -water enum spc
        Water model to use: with GROMOS we recommend SPC,  with  OPLS,  TIP4P:
       spc,  spce,  tip3p,  tip4p,  tip5p or  f3c

       -[no]interno
        Set the next 8 options to interactive

       -[no]ssno
        Interactive SS bridge selection

       -[no]terno
        Interactive termini selection, iso charged

       -[no]lysno
        Interactive Lysine selection, iso charged

       -[no]argno
        Interactive Arganine selection, iso charged

       -[no]aspno
        Interactive Aspartic Acid selection, iso charged

       -[no]gluno
        Interactive Glutamic Acid selection, iso charged

       -[no]glnno
        Interactive Glutamine selection, iso neutral

       -[no]hisno
        Interactive Histidine selection, iso checking H-bonds

       -angle real 135
        Minimum hydrogen-donor-acceptor angle for a H-bond (degrees)

       -dist real 0.3
        Maximum donor-acceptor distance for a H-bond (nm)

       -[no]unano
        Select   aromatic   rings  with  united  CH  atoms  on  Phenylalanine,
       Tryptophane and Tyrosine

       -[no]ignhno
        Ignore hydrogen atoms that are in the pdb file

       -[no]missingno
        Continue when atoms are missing, dangerous

       -[no]vno
        Be slightly more verbose in messages

       -posrefc real 1000
        Force constant for position restraints

       -vsite enum none
        Convert atoms to virtual sites:  none,  hydrogens or  aromatics

       -[no]heavyhno
        Make hydrogen atoms heavy

       -[no]deuterateno
        Change the mass of hydrogens to 2 amu

SEE ALSO

       gromacs(7)

       More     information     about     GROMACS     is     available      at
       <http://www.gromacs.org/>.

                                Thu 16 Oct 2008                     pdb2gmx(1)