Provided by: gromacs-data_2024.2-1_all 
NAME
gmx-dssp - Calculate protein secondary structure via DSSP algorithm
SYNOPSIS
gmx dssp [-f [<.xtc/.trr/...>]] [-s [<.tpr/.gro/...>]] [-n [<.ndx>]]
[-o [<.dat>]] [-num [<.xvg>]] [-b <time>] [-e <time>]
[-dt <time>] [-tu <enum>] [-fgroup <selection>]
[-xvg <enum>] [-[no]rmpbc] [-[no]pbc] [-sf <file>]
[-selrpos <enum>] [-seltype <enum>] [-sel <selection>]
[-hmode <enum>] [-hbond <enum>] [-[no]nb] [-cutoff <real>]
[-[no]clear] [-[no]pihelix] [-ppstretch <enum>]
DESCRIPTION
gmx dssp allows using the DSSP algorithm (namely, by detecting specific patterns of hydrogen bonds
between amino acid residues) to determine the secondary structure of a protein.
One-symbol secondary structure designations that are used in the output file:
H — alpha-helix;
B — residue in isolated beta-bridge;
E — extended strand that participates in beta-ladder;
G — 3_10-helix;
I — pi-helix;
P — kappa-helix (poly-proline II helix);
S — bend;
T — hydrogen-bonded turn;
= — break;
~ — loop (no special secondary structure designation).
-num allows you to get a plot of the number of secondary structures of each type as a function of time at
the output.
-hmode selects between using hydrogen atoms directly from the structure ("gromacs" option) and using
hydrogen pseudo-atoms based on C and O atom coordinates of previous residue ("dssp" option). You should
always use the "dssp" option for structures with absent hydrogen atoms!
-hbond selects between different definitions of hydrogen bond. "energy" means the calculation of a
hydrogen bond using the electrostatic interaction energy and "geometry" means the calculation of the
hydrogen bond using geometric criterion for the existence of a hydrogen bond.
-nb allows using GROMACS neighbor-search method to find residue pairs that may have a hydrogen bond
instead of simply iterating over the residues among themselves.
-cutoff is a real value that defines maximum distance from residue to its neighbor residue used in -nb.
Minimum (and also recommended) value is 0.9.
-clear allows you to ignore the analysis of the secondary structure residues that are missing one or more
critical atoms (CA, C, N, O or H). Always use this option together with -hmode dssp for structures that
lack hydrogen atoms!
-pihelix changes pattern-search algorithm towards preference of pi-helices.
-ppstretch defines stretch value of polyproline-helices. "shortened" means stretch with size 2 and
"default" means stretch with size 3.
Note that gmx dssp currently is not capable of reproducing the secondary structure of proteins whose
structure is determined by methods other than X-ray crystallography (structures in .pdb format with
incorrect values in the CRYST1 line) due to the incorrect cell size in such structures.
Please note that the computation is always done in single precision, regardless of the precision for
which GROMACS was configured.
OPTIONS
Options to specify input files:
-f [<.xtc/.trr/...>] (traj.xtc) (Optional)
Input trajectory or single configuration: xtc trr cpt gro g96 pdb tng
-s [<.tpr/.gro/...>] (topol.tpr) (Optional)
Input structure: tpr gro g96 pdb brk ent
-n [<.ndx>] (index.ndx) (Optional)
Extra index groups
Options to specify output files:
-o [<.dat>] (dssp.dat)
Filename for DSSP output
-num [<.xvg>] (num.xvg) (Optional)
Output file name for secondary structures statistics for the trajectory
Other options:
-b <time> (0)
First frame (ps) to read from trajectory
-e <time> (0)
Last frame (ps) to read from trajectory
-dt <time> (0)
Only use frame if t MOD dt == first time (ps)
-tu <enum> (ps)
Unit for time values: fs, ps, ns, us, ms, s
-fgroup <selection>
Atoms stored in the trajectory file (if not set, assume first N atoms)
-xvg <enum> (xmgrace)
Plot formatting: xmgrace, xmgr, none
-[no]rmpbc (yes)
Make molecules whole for each frame
-[no]pbc (yes)
Use periodic boundary conditions for distance calculation
-sf <file>
Provide selections from files
-selrpos <enum> (atom)
Selection reference positions: atom, res_com, res_cog, mol_com, mol_cog, whole_res_com,
whole_res_cog, whole_mol_com, whole_mol_cog, part_res_com, part_res_cog, part_mol_com,
part_mol_cog, dyn_res_com, dyn_res_cog, dyn_mol_com, dyn_mol_cog
-seltype <enum> (atom)
Default selection output positions: atom, res_com, res_cog, mol_com, mol_cog, whole_res_com,
whole_res_cog, whole_mol_com, whole_mol_cog, part_res_com, part_res_cog, part_mol_com,
part_mol_cog, dyn_res_com, dyn_res_cog, dyn_mol_com, dyn_mol_cog
-sel <selection>
Group for DSSP
-hmode <enum> (gromacs)
Hydrogens pseudoatoms creating mode: gromacs, dssp
-hbond <enum> (energy)
Selects between different definitions of hydrogen bond: energy, geometry
-[no]nb (yes)
Use GROMACS neighbor-search method
-cutoff <real> (0.9)
Distance from residue to its neighbor residue in neighbor search. Must be >= 0.9
-[no]clear (no)
Clear defective residues from the structure
-[no]pihelix (no)
Prefer Pi Helices
-ppstretch <enum> (default)
Stretch value for PP-helices: shortened, default
SEE ALSO
gmx(1)
More information about GROMACS is available at <http://www.gromacs.org/>.
COPYRIGHT
2024, GROMACS development team
2024.2 May 10, 2024 GMX-DSSP(1)