Trajectory SP277
Force field:
martini_v2.2
Simulation length (ns): 5000
Electric field (kJ mol-1 nm-1 e-1): 0
Temperature (K): 300 (v-rescale)
Pressure (bar): 1 (parrinello-rahman semiisotropic)
Number of particles: 24407
Time step (fs) : 25
Software: GROMACS 2020
Simulation length (ns): 5000
Electric field (kJ mol-1 nm-1 e-1): 0
Temperature (K): 300 (v-rescale)
Pressure (bar): 1 (parrinello-rahman semiisotropic)
Number of particles: 24407
Time step (fs) : 25
Software: GROMACS 2020
Supercomputer:
Finisterrae II CESGA
Peptides: P47 NC00004
Lipids: DOPC, DOPE, DOPS, DPSM
Heteromolecules: CHOL
Ions: NA
Water model: W
Peptides: P47 NC00004
Lipids: DOPC, DOPE, DOPS, DPSM
Heteromolecules: CHOL
Ions: NA
Water model: W
Sequence :
GCCSNPVCFATHSNLC
Total charge (e): 0
Number of residues: 16
By amino acid: Basic: 1 Acidic: 0 Hydrophobic: 6 Polar: 9 Electrostatic Dipolar Moment (e nm): 2.46
Longitudinal (e nm): 2.46 Transversal (e nm): 0 Hydrophobic Dipolar Moment (nm): 0.8
Longitudinal (nm): 0.47 Transversal (nm): 0.65 Secondary structure: Helix
Activity:
Download Files
ITP file. JSON file. PDB file.
Click on any component to highlight it from the plot.
Upper leaflet
Lower leaflet
Lipids
Membrane model for: DOPC:DOPE:DOPS:DPSM:CHOL (3:3:3:2:4) (Cancer)
DOPC
1,2-dioleoyl-sn-glycero-3-phosphocholine
Total charge (e): 0
See DOPC lipid
Download ITP File. Download PDB File.
DOPE
1,2-dioleoyl-sn-glycero-3-phosphoethanolamine
Total charge (e): 0
See DOPE lipid
Download ITP File. Download PDB File.
DOPS
1,2-dioleoyl-sn-glycero-3-phospho-L-serine
Total charge (e): -1
See DOPS lipid
Download ITP File. Download PDB File.
Last snapshot
Total contacts per residue
Number of total contacts per residue type:
Number of contacts between each residue of the peptide backbone and the different lipid types, averaged over the last microsecond and using a cut-off of 0.6 nm.
Contacts per residue
(normalized by total number of beads of the amino acid):
Number of contacts between each residue of the peptide backbone and the different lipid types, averaged over the last microsecond and using a cut-off of 0.6 nm.
Molecular Dynamics based descriptors
Average and standard deviation,
calculated using the autocorrelation function (for time
series)
or the width of the distribution, for the last microsecond
of
the trajectory
Area per lipid
Membrane (nm2): 0.71432 ± 0.00081
Upper leaflet (nm2): 0.71432 ± 0.00081
Lower leaflet (nm2): 0.71432 ± 0.00081
Average Z coordinate
Peptide (nm): 12.869 ± 0.035
First Residue (nm): 12.830 ± 0.051
Last Residue (nm): 13.107 ± 0.052
Membrane (nm): 10.836 ± 0.012
Upper leaflet Head Group (nm): 12.834 ± 0.013
Lower leaflet Head Group (nm): 8.838 ± 0.011
Bilayer Thickness (nm): 3.996 ± 0.017
Peptide insertion (nm): 0.035 ± 0.037
Contacts
Peptide - Water: 25.02 ± 0.52
Peptide - Head groups: 8.92 ± 0.18
Peptide - Tail groups: 7.46 ± 0.23
Tilt (°): 82.3 ± 2.0
Membrane (nm2): 0.71432 ± 0.00081
Upper leaflet (nm2): 0.71432 ± 0.00081
Lower leaflet (nm2): 0.71432 ± 0.00081
Average Z coordinate
Peptide (nm): 12.869 ± 0.035
First Residue (nm): 12.830 ± 0.051
Last Residue (nm): 13.107 ± 0.052
Membrane (nm): 10.836 ± 0.012
Upper leaflet Head Group (nm): 12.834 ± 0.013
Lower leaflet Head Group (nm): 8.838 ± 0.011
Bilayer Thickness (nm): 3.996 ± 0.017
Peptide insertion (nm): 0.035 ± 0.037
Contacts
Peptide - Water: 25.02 ± 0.52
Peptide - Head groups: 8.92 ± 0.18
Peptide - Tail groups: 7.46 ± 0.23
Tilt (°): 82.3 ± 2.0
PepDF:
5(ns): CVS
Displacement (nm): 0.799 ± 0.056
Precession(°): 1.6 ± 2.9
50(ns) CVS
Displacement (nm): 2.58 ± 0.46
Precession(°): 16.0 ± 20.0
100(ns) CVS
Displacement(nm): 3.69 ± 0.94
Precession(°): 29.0 ± 31.0
200(ns) CVS
Displacement(nm): 5.6 ± 2.5
Precession(°): 62.0 ± 42.0
Download JSON File.
5(ns): CVS
Displacement (nm): 0.799 ± 0.056
Precession(°): 1.6 ± 2.9
50(ns) CVS
Displacement (nm): 2.58 ± 0.46
Precession(°): 16.0 ± 20.0
100(ns) CVS
Displacement(nm): 3.69 ± 0.94
Precession(°): 29.0 ± 31.0
200(ns) CVS
Displacement(nm): 5.6 ± 2.5
Precession(°): 62.0 ± 42.0
Download JSON File.
Peptide Analyses
Peptide Displacement Fingerprint
(PepDF)
Lateral displacement vs
Rotational
Displacement along the trajectory, for different time
windows .
Tilt angle: 
Peptide tilt angle evolution, defined as the angle between the peptide helical axis and the bilayer normal .
Peptide spin: 
Evolution of the angle formed by the transversal component of the hydrophobic dipolar moment and a vector transversal to the peptide pointing outwards the membrane.
Lipid Analyses:
Area per lipid
In this system both leaflets have the same number of lipids, thus the values for their APL are overlaping in the plot
Density maps:
2D-density maps of lipids around the
peptide
along XY and YZ axis, calculated for each lipid type along the
last
microsecond.
Lipid-Peptide Analyses:
z-Position
Z-coordinate, averaged for
differetn
parts of the the system: peptide, membrane, first and
last
backbone (BB) residues and upper of lower leaflet
lipids’
headgroups (HGs).
Minimum distance
Minimum distance (nm) between the
peptide backbone and the lipids (headgroups and
tailgroups).
Number of contacts
Number of contacts between the
peptide backbone and the water or the lipids separated
by
lipid headgroups (HG) or lipid tails, using a cut-off of
0.6
nm.
Lateral density
Lateral density for the different
components of the system: headgroups, tail groups,
peptide
and water.