Example input files and purpose:

 
Purpose:  Illustrate a few CHARMM fundamentals

Usage:

%  charmm <  tutorial.inp  >   tutorial.out
%  charmm <  tutorial2.inp >  tutorial2.out
 

• General tutorial and overview
1. tutorial.inp

tutorial2.inp
 
Required files: none

• Initial conditioning and solvation of protein structure

1. protein-generate_solvate.inp


Purpose:  Provide an initial set-up of protein psf (with or without solvation)

Usage:

% charmm pdbfile=1spz  solvate=true crystal=true shape=octahedral {toppar=$toppar seqname=1spz psf=false cutoff=9} < input/protein-generate_solvate.inp > output/protein-generate.out

Required files: $toppar/top_all22_prot.inp, $toppar/par_all22_prot.inp, ./coor/@pdbfile.pdb, ./data/tip125.crd, ./data/tip216.crd, ./data/octa.img
 

Where: {...} means these are default values and don't need to be specified.
!*   toppar   ($toppar)  ==> path to parameter and topology files
!**
!*   pdbfile     (...)   ==> name of pdb coordinate file containing
!**                          coordinates and sequence information
!**                          (for psf=true key this is the name of the
!**                          coordinate file in pdb format (pdbfile_minimized.pdb)
!**                          and the pre-generated psf file (pdbfile.psf))
!*   psf       (false)   ==> key specifying use of pre-generated psf and
!**                          pdb coordinate file for use w/ multi-segid
!**                          solute systems
!*   seqname  (pdbfile)  ==> name of protein sequence (segid)
!**
!*   shape      (cubic)  ==> variable specifying whether truncated octahedral or
!**                          cubic volume used (octahedral/cubic)
!*   crystal    (false)  ==> logical variable true/false specifying whether
!**                          to use crystal orientation of simulation volume
!*   cutoff      (9)    ==> value of cutoff to be used in establishing how
!**                          far images are to be from volume "edges", often set
!**                          at or near nonbonded list cutoff value
!**                          to use crystal orientation of simulation volume
!*   solvate    (false) ==> logical flag which determines whether you stop after
!**                          initial minimization and psf generation or proceed

• Initial conditioning and solvation of  DNA structure

1. DNA-ions-n-solvate.inp

Purpose:  Provide an initial set-up of DNA + Na+ counter ions  psf (with or without solvation)

Usage:
charmm pdbfile=103d  solvate=true crystal=true shape=cubic {toppar=$toppar seqname=103d psf=false cutoff=9} < input/DNA-ions-n-solvate.inp > output/DNA-ions-n-solvate.out

Required files: $toppar/top_all22_na.inp, $toppar/par_all22_na.inp, ./coor/@pdbfile.pdb, ./data/tip125.crd, ./data/tip216.crd, ./data/octa.img

Where: {...} means these are default values and don't need to be specified.

!*   toppar   ($toppar)  ==> path to parameter and topology files
!**
!*   pdbfile     (...)   ==> name of pdb coordinate file containing
!**                          coordinates and sequence information
!**                          (for psf=true key this is the name of the
!**                          coordinate file in pdb format (pdbfile_minimized.pdb)
!**                          and the pre-generated psf file (pdbfile.psf))
!*   psf       (false)   ==> key specifying use of pre-generated psf and
!**                          pdb coordinate file for use w/ multi-segid
!**                          solute systems
!*   shape      (cubic)  ==> variable specifying whether truncated octahedral or
!**                          cubic volume used (octahedral/cubic)
!*   crystal    (false)  ==> logical variable true/false specifying whether
!**                          to use crystal orientation of simulation volume
!*   cutoff      (9)    ==> value of cutoff to be used in establishing how
!**                          far images are to be from volume "edges", often set
!**                          at or near nonbonded list cutoff value
!**                          to use crystal orientation of simulation volume
!*   solvate    (false) ==> logical flag which determines whether you stop after
!**                          initial minimization and psf generation or proceed

• Estimate of pKa values for protein residues using single site approximation with generalized Born and/or Poisson-Boltzmann continuum approximations.

1. protein-pKa.inp

Purpose:  Calculate estimates of deltapKa values for protein or peptide

Usage:
charmm pdbfile=1hel minimize=false epsinterior=10 pb=false size=0.75 < input/protein-pKa.inp > output/protein-pKa.out (illustrate GB pKa calculation for whole protein)

charmm pdbfile=phel minimize=false epsinterior=10 pb=false size=0.75 < input/protein-pKa.inp > output/protein-pKa_pb.out (illustrate GB & PB pKa calculation for protein fragment)
 

Required files: $toppar/top_all22_prot.inp, $toppar/par_all22_prot.inp, ./coor/@pdbfile.pdb

Where: {...} means these are default values and don't need to be specified.

!*   toppar   ($toppar)  ==> path to parameter and topology files
!**
!*   pdbfile     (...)   ==> name of pdb coordinate file containing
!**                          coordinates and sequence information
!**
!*   minimize    (false) ==> logical determining whether to condition
!**                          pdb structure by minimization or not
!**
!*   epsinterior (10)    ==> value to sue for protein interior dielectric
!**                          constant
!*   pb         (false)  ==> logical indicating whether to use Poisson-Boltzmann
!**                          continuum model to do pKa calculation
!*   size        (0.75)  ==> grid spacing to use in finite difference PB
!**                          calculation

 

• Free energy perturbation methods - mutation of protein residue (Y33F)

1. protein_FEP-by-TSM.inp

Purpose:  Illustrate calculation of free energy differences for perturbation of amino acid residue in
protein and reference (peptide) state using CHARMM TSM (Thermodynamic Simulation Modeule).

Usage:
charmm pdbfile=1pgb  resnum=33 lambdastep=0.3 dynamics=true analysis=true < input/protein_FEP-by-TSM.inp > output/protein_FEP-by-TSM.out (perturbation in protein)

charmm pdbfile=rpgb  resnum=33 lambdastep=0.3 dynamics=true analysis=true < input/protein_FEP-by-TSM.inp > output/protein_FEP-by-TSM_ref.out (perturbation in reference peptide)

Required files: $toppar/top_all22_prot.inp, $toppar/par_all22_prot.inp, ./coor/@pdbfile.pdb

Where: {...} means these are default values and don't need to be specified.

!*   toppar   ($toppar)  ==> path to parameter and topology files
!**
!*   pdbfile     (...)   ==> name of pdb coordinate file containing
!**                          coordinates and sequence information
!**                          (for psf=true key this is the name of the
!**                          coordinate file in pdb format (pdbfile.pdb)
!**                          and the pre-generated psf file (pdbfile.psf))
!*   psf       (false)   ==> key specifying use of pre-generated psf and
!**                          pdb coordinate file for use w/ multi-segid
!**                          solute systems
!*   resnum     (33)     ==> residue number of mutation site
!*   lambdastep (0.1)    ==> stepsize for FEP perturbations
!*   dynamics   (false)  ==> logical determining whether FEP
!**                          simulation to be performed
!*   analysis   (false)  ==> logical determining whether analysis of FEP
!**                          simulation to be performed

• Results:

• Approximate association free energy for leucine zipper

1. 2zta_bind-w-GB.inp

Purpose:  Illustrate the GB/MM approach to estimating free energy difference for two examples.  1) Association energy of leucine zipper dimer from analysis of native 2zta leucine zipper trajectory.  2) Association energy for Asn16Ala mutant of leucine zipper 2zta computed from same trajectory ("alanine scanning").

Usage:
charmm N2A=false pdbfile=1pgb  < input/2zta_bind-w-GB.inp > output/2zta_bind-w-GB.out (association in native leucine zipper)

charmm N2A=false pdbfile=1pgb  < input/2zta_bind-w-GB.inp > output/2zta_bind-w-GB_N2A.out (association in mutant leucine zipper)

Required files: $toppar/toph19.inp, $toppar/param19.inp, ./crd/2zta_d1-60p-sub.hex
 

• Results: