def test_search(universe):
"""simply check that for a centered protein in a large box pkdtree
and kdtree return the same result"""
ns = NeighborSearch.AtomNeighborSearch(universe.atoms)
pns = NeighborSearch.AtomNeighborSearch(universe.atoms,
universe.atoms.dimensions)
ns_res = ns.search(universe.atoms[20], 20)
pns_res = pns.search(universe.atoms[20], 20)
assert_equal(ns_res, pns_res)
def notwithin_coordinates(cutoff=cutoff):
# acts as '<solvent> WITHIN <cutoff> OF <protein>'
# must update every time step
ns_w = NS.AtomNeighborSearch(
solvent) # build kd-tree on solvent (N_w > N_protein)
group = ns_w.search(protein,
cutoff) # solvent within CUTOFF of protein
return group.positions
def notwithin_coordinates(cutoff=cutoff):
# must update every time step
ns_w = NS.AtomNeighborSearch(solvent) # build kd-tree on solvent (N_w > N_protein)
solvation_shell = ns_w.search(protein, cutoff) # solvent within CUTOFF of protein
# Find indices in solvent NOT in solvation shell
uniq_idx = np.setdiff1d(solvent.ix, solvation_shell.ix)
# Then reselect these from Universe.atoms (as these indices are global)
group = universe.atoms[uniq_idx]
return group.positions
def notwithin_coordinates(cutoff=cutoff):
# must update every time step
ns_w = NS.AtomNeighborSearch(
solvent) # build kd-tree on solvent (N_w > N_protein)
solvation_shell = ns_w.search_list(
protein, cutoff) # solvent within CUTOFF of protein
group = MDAnalysis.core.AtomGroup.AtomGroup(
set_solvent - set(solvation_shell)) # bulk
return group.coordinates()
def find_clashing_rotamers(self, fitted_rotamers, protein, site_resid):
"""Detect any rotamer that clashes with the protein."""
# make a KD tree of the protein neighbouring atoms
proteinNotSite = protein.select_atoms("protein and not name H* and not (resid " + str(site_resid) +
" or (resid " + str(site_resid-1) + " and (name C or name O)) "
"or (resid " + str(site_resid+1)
+ " and name N))")
proteinNotSiteLookup = KDNS.AtomNeighborSearch(proteinNotSite)
rotamerSel = fitted_rotamers.select_atoms("not name H*")
rotamer_clash = []
for rotamer in fitted_rotamers.trajectory:
bumps = proteinNotSiteLookup.search(rotamerSel, self.clashDistance)
rotamer_clash.append(bool(bumps))
return rotamer_clash, np.sum(rotamer_clash)
def analysis(lUniverses, searchAtoms, radius, fileName):
#Inputs:
# a list of MD Analysis Universes,
# a search string (in MD Analysis atom selection grammar)
# Radius (in Angstroms) around the search atoms in which to search
# string to call the analysis result file
#Outputs:
# a pickle file containing a list of dictionaries with the results in the following format:
# [{information about a residue that is whithin the search radius}, {}, {}, {}]
resList = []
for u in lUniverses:
SearchClass = NSearch.AtomNeighborSearch(u.atoms)
nr = []
for ts in u.trajectory:
nr.append(
SearchClass.search(u.select_atoms(searchAtoms), radius, 'R'))
nr = np.array(nr)
for a in range(len(nr)):
for i in range(len(nr[a])):
resList.append(nr[a][i])
resList = np.array(resList)
unRes = np.unique(resList, return_counts=True)
unRes = np.array(unRes)
unRes = unRes.T
unRes = unRes[np.argsort(unRes[:,
1])] #sorts into ascending order of counts
unRes = np.flip(unRes, axis=0) # flips to descending order of counts
lResidues = []
for i in range(1, len(unRes)):
dRes = {}
dRes['segid'] = unRes[i][0].segid
dRes['resname'] = unRes[i][0].resname
dRes['resid'] = unRes[i][0].resid
dRes['count'] = unRes[i][1]
dRes['countPercentage'] = unRes[i][1] / len(lUniverses[0].trajectory)
dRes['full_string'] = str(dRes['segid']) + " " + str(
dRes['resname']) + " " + str(dRes['resid'])
lResidues.append(dRes)
save(lResidues, fileName)
def find_clashing_rotamers(clash_distance, rotamer_site, protein, resid,
chainid):
"""
Detect any rotamer that clashes with the protein.
Parameters
----------
clash_distance: float
distance between atoms of the spin-spin label and the protein
rotamer_site:
trajectory of rotamer states attached to spin-label position
protein: pdb
resid: int
spin-labeled position
chainid: string
chain of the spin-labeled position
Returns
-------
rotamer_clash: array
For each spin-label position, an array with boolean entries
of each rotameric state (True: clash, False: no clash)
"""
# make a KD tree of the protein neighbouring atoms
proteinNotSite = protein.select_atoms(
"protein and not name H* and not (resid " + str(resid) +
" or (resid " + str(resid - 1) + " and (name C or name O)) "
"or (resid " + str(resid + 1) + " and name N))")
proteinNotSiteLookup = KDNS.AtomNeighborSearch(proteinNotSite)
rotamerSel = rotamer_site.select_atoms("not name H*")
rotamer_clash = []
for rotamer in rotamer_site.trajectory:
bumps = proteinNotSiteLookup.search(rotamerSel, clash_distance)
rotamer_clash.append(bool(bumps))
return rotamer_clash
def analyze_clusters(frame):
u = MDAnalysis.Universe(gro,xtc)
print('Frame %i of %i......'%(frame,u.trajectory.n_frames))
start = time.time()
u.trajectory[frame]
######## Discriminate between leaflets in this frame to construct leaflet-separated groups
#Lipid Residue names
lipid1 ='DPPC'
lipid2 ='DIPC'
lipid3 ='CHOL'
lpd1_atoms = u.select_atoms('resname %s and name PO4'%lipid1)
lpd2_atoms = u.select_atoms('resname %s and name PO4'%lipid2)
lpd3_atoms = u.select_atoms('resname %s and name ROH'%lipid3)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# atoms in the upper leaflet as defined by insane.py or the CHARMM-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
lpd1i_up = lpd1_atoms[:((num_lpd1)/2)]
lpd2i_up = lpd2_atoms[:((num_lpd2)/2)]
lipids_up = lpd1i_up + lpd2i_up
ns_lipids_up = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i_up = ns_lipids_up.search(lipids_up,15.0)
lpd3i_up_resids = np.unique(lpd3i_up.resids)
lpd1i_down = lpd1_atoms[((num_lpd1)/2):]
lpd2i_down = lpd2_atoms[((num_lpd2)/2):]
lipids_down = lpd1i_down + lpd2i_down
ns_lipids_down = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i_down = ns_lipids_down.search(lipids_down,15.0)
lpd3i_down_resids = np.unique(lpd3i_down.resids)
# ID center of geometry coordinates for cholesterol on indicated bilayer side
lpd3_up_coords = np.zeros((len(lpd3i_up.resnums),3))
for i in np.arange(len(lpd3i_up.resnums)):
resnum = lpd3i_up.resnums[i]
group = u.select_atoms('resnum %i and (name R1 or name R2 or name R3 or name R4 or name R5)'%resnum)
group_cog = group.center_of_geometry()
lpd3_up_coords[i] = group_cog
lpd3_down_coords = np.zeros((len(lpd3i_down.resnums),3))
for i in np.arange(len(lpd3i_down.resnums)):
resnum = lpd3i_down.resnums[i]
group = u.select_atoms('resnum %i and (name R1 or name R2 or name R3 or name R4 or name R5)'%resnum)
group_cog = group.center_of_geometry()
lpd3_down_coords[i] = group_cog
# ID coordinates for lipids on indicated bilayer side, renaming variables
lpd1_atoms = u.select_atoms('resname %s and (name C2A or name C2B)'%lipid1)
lpd2_atoms = u.select_atoms('resname %s and (name D2A or name D2B)'%lipid2)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# select lipid tail atoms beloging to the selected bilayer side
lpd1i_up = lpd1_atoms[:((num_lpd1)/2)]
lpd2i_up = lpd2_atoms[:((num_lpd2)/2)]
lpd1i_down = lpd1_atoms[((num_lpd1)/2):]
lpd2i_down = lpd2_atoms[((num_lpd2)/2):]
# assign lpd1 coordinates, completing the assignment of all coordinates from which psi6 will be computed
lpd1_up_coords = lpd1i_up.coordinates()
lpd2_up_coords = lpd2i_up.coordinates()
lpd1_down_coords = lpd1i_down.coordinates()
lpd2_down_coords = lpd2i_down.coordinates()
lpd_up_coords = np.vstack((lpd1_up_coords,lpd3_up_coords))
lpd_up_coords = lpd_up_coords.astype('float32')
lpd_up_full_coords = np.vstack((lpd1_up_coords,lpd3_up_coords,lpd2_up_coords)) # un-evaluated indices will go last
lpd_up_full_coords = lpd_up_full_coords.astype('float32')
lpd_down_coords = np.vstack((lpd1_down_coords,lpd3_down_coords))
lpd_down_coords = lpd_down_coords.astype('float32')
lpd_down_full_coords = np.vstack((lpd1_down_coords,lpd3_down_coords,lpd2_down_coords)) # un-evaluated indices will go last
lpd_down_full_coords = lpd_down_full_coords.astype('float32')
# Select tail atoms for M inter-leaflet cluster analysis
lpd1_tail_atoms = u.select_atoms('resname %s and (name C4A or name C4B)'%lipid1)
num_tail_lpd1 = lpd1_tail_atoms.n_atoms
lpd1i_tail_up = lpd1_tail_atoms[:((num_tail_lpd1)/2)]
lpd1i_tail_down = lpd1_tail_atoms[((num_tail_lpd1)/2):]
lpd3i_tail_up = []
for resid in lpd3i_up_resids:
sel = u.select_atoms('resid %i and name C2'%resid)
lpd3i_tail_up.append(sel)
lpd3i_tail_up = np.sum(lpd3i_tail_up)
lpd3i_tail_down = []
for resid in lpd3i_down_resids:
sel = u.select_atoms('resid %i and name C2'%resid)
lpd3i_tail_down.append(sel)
lpd3i_tail_down = np.sum(lpd3i_tail_down)
tail_up = lpd1i_tail_up + lpd3i_tail_up
tail_down = lpd1i_tail_down + lpd3i_tail_down
########################################################################################
resids_up = np.concatenate([lpd1i_up.resids, np.unique(lpd3i_up.resids)])
resids_down = np.concatenate([lpd1i_down.resids, np.unique(lpd3i_down.resids)])
c = u.trajectory.ts.triclinic_dimensions[0][0] # box length
box = u.trajectory.ts.triclinic_dimensions
up_cluster_groups = extract_clusters(lpd_up_coords, c, resids_up)
down_cluster_groups = extract_clusters(lpd_down_coords, c, resids_down)
N_absPsi6s = []
N_p2s = []
N_c_sizes = []
#Compute structural parameters for n -- intra-leaflet cluster parameters on both sides
haystack = lpd1i_up.indices
for group in up_cluster_groups:
if group.select_atoms('resname DPPC').n_residues != 0: # only evaluate DPPC-containing clusters
# do structural analysis and save the cluster size
p2 = compute_p2s(group) # mean P2 for the cluster
c_size = group.select_atoms('name C4A or name C4B or name C2').n_atoms # the number of carbon chains in the cluster
N_p2s.append(p2)
N_c_sizes.append(c_size)
# do psi6 ONLY for dppc molecules
packed = group.select_atoms('resname %s and (name C2A or name C2B)'%lipid1)
needles = packed.indices
st = set(needles)
atomindices = [i for i, e in enumerate(haystack) if e in st]
absPsi6 = np.mean(np.abs(get_psi6(lpd_up_full_coords, atomindices, box)))
N_absPsi6s.append(absPsi6)
print('finished upper leaflet intra-leaflet clustering, n!')
haystack = lpd1i_down.indices
for group in down_cluster_groups:
if group.select_atoms('resname DPPC').n_residues != 0: # only evaluate DPPC-containing clusters
# do structural analysis and save the cluster size
p2 = compute_p2s(group) # mean P2 for the cluster
c_size = group.select_atoms('name C4A or name C4B or name C2').n_atoms # the number of carbon chains in the cluster
N_p2s.append(p2)
N_c_sizes.append(c_size)
# do psi6 ONLY for dppc molecules
packed = group.select_atoms('resname %s and (name C2A or name C2B)'%lipid1)
needles = packed.indices
st = set(needles)
atomindices = [i for i, e in enumerate(haystack) if e in st]
absPsi6 = np.mean(np.abs(get_psi6(lpd_down_full_coords, atomindices, box)))
N_absPsi6s.append(absPsi6)
print('finished lower leaflet intra-leaflet clustering, n!')
M_absPsi6s = []
M_p2s = []
M_c_sizes = []
# Compute structural parameters for m -- inter-leaflet cluster parameters on both sides
haystack = lpd1i_down.indices
for group in up_cluster_groups:
if group.select_atoms('resname DPPC').n_residues != 0: # only evaluate DPPC-containing clusters
# find the residue ids of the inter-leaflet DPPC molecules within M_cutoff ang of molecules in the cluster
ns_inter_lipids = NS.AtomNeighborSearch(lpd1i_tail_down) # using inter-leaflet DPPC molecules....
inter_lipids = ns_inter_lipids.search(group, M_cutoff) # find inter-leaflet DPPC molecules
# find the residue ids of the inter-leaflet DPPC and CHOL molecules within M_cutoff ang of molecules in the cluster
ns_inter_atoms = NS.AtomNeighborSearch(tail_down) # using inter-leaflet DPPC and CHOL molecules....
inter_atoms = ns_inter_atoms.search(group, M_cutoff) # find inter-leaflet DPPC and CHOL molecules
if inter_atoms != []:
c_size = inter_atoms.n_atoms
M_c_sizes.append(c_size)
else:
M_c_sizes.append(0)
if inter_lipids != []:
inter_lipids_resids = np.unique(inter_lipids.resids)
inter_lipid_groups = []
for resid in inter_lipids_resids:
sel = u.select_atoms('resid %i'%resid)
inter_lipid_groups.append(sel)
inter_group = np.sum(inter_lipid_groups)
p2 = compute_p2s(inter_group)
M_p2s.append(p2)
# do psi6 ONLY for dppc molecules
packed = inter_group.select_atoms('resname %s and (name C2A or name C2B)'%lipid1)
needles = packed.indices
st = set(needles)
atomindices = [i for i, e in enumerate(haystack) if e in st]
absPsi6 = np.mean(np.abs(get_psi6(lpd_down_full_coords, atomindices, box)))
M_absPsi6s.append(absPsi6)
else:
M_p2s.append(0)
M_absPsi6s.append(0)
print('finished upper leaflet inter-leaflet clustering, m!')
haystack = lpd1i_up.indices
for group in down_cluster_groups:
if group.select_atoms('resname DPPC').n_residues != 0: # only evaluate DPPC-containing clusters
# find the residue ids of the inter-leaflet DPPC molecules within 10 ang of molecules in the cluster
ns_inter_lipids = NS.AtomNeighborSearch(lpd1i_tail_up) # using inter-leaflet DPPC molecules....
inter_lipids = ns_inter_lipids.search(group, M_cutoff) # find inter-leaflet DPPC molecules within 10 ang of the cluster
# find the residue ids of the inter-leaflet DPPC and CHOL molecules within M_cutoff ang of molecules in the cluster
ns_inter_atoms = NS.AtomNeighborSearch(tail_up) # using inter-leaflet DPPC and CHOL molecules....
inter_atoms = ns_inter_atoms.search(group, M_cutoff) # find inter-leaflet DPPC and CHOL molecules
if inter_atoms != []:
c_size = inter_atoms.n_atoms
M_c_sizes.append(c_size)
else:
M_c_sizes.append(0)
if inter_lipids != []:
inter_lipids_resids = np.unique(inter_lipids.resids)
inter_lipid_groups = []
for resid in inter_lipids_resids:
sel = u.select_atoms('resid %i'%resid)
inter_lipid_groups.append(sel)
inter_group = np.sum(inter_lipid_groups)
p2 = compute_p2s(inter_group)
M_p2s.append(p2)
# do psi6 ONLY for dppc molecules
packed = inter_group.select_atoms('resname %s and (name C2A or name C2B)'%lipid1)
needles = packed.indices
st = set(needles)
atomindices = [i for i, e in enumerate(haystack) if e in st]
absPsi6 = np.mean(np.abs(get_psi6(lpd_up_full_coords, atomindices, box)))
M_absPsi6s.append(absPsi6)
else:
M_p2s.append(0)
M_absPsi6s.append(0)
print('finished lower leaflet inter-leaflet clustering, m!')
N_c_sizes = np.array(N_c_sizes)
N_p2s = np.array(N_p2s)
N_absPsi6s = np.array(N_absPsi6s)
M_c_sizes = np.array(M_c_sizes)
M_p2s = np.array(M_p2s)
M_absPsi6s = np.array(M_absPsi6s)
#results.append( [N_c_sizes, M_c_sizes, N_p2s, M_p2s, N_absPsi6s, M_absPsi6s] )
print('This whole process ran for', time.time()-start)
return N_c_sizes, M_c_sizes, N_p2s, M_p2s, N_absPsi6s, M_absPsi6s
def cluster_analysis(self,
cut_off=7.5,
times=None,
style="atom",
measure="b2b",
algorithm="dynamic",
work_in="Residue",
traj_pbc_style=None,
pbc=True):
"""High level function clustering molecules together
Example
-------
No Example yet
Note
----
Not all of the functionality is actually coded yet
Parameters
----------
cut_off : float, optional
Minimal distance for two particles to be in the
same cluster, in Angstroem. Results still depend
on the measure parameter.
time : list of floats, optional
If None, do for whole trajectory. If an interval
is given like this (t_start, t_end) only do from start
to end.
style : string, optional
"atom" or "molecule". Dependent on this, the
cluster_objects attribute is interpreted as molecule
or atoms within a molecule.
measure : string, optional
"b2b (bead to bead), COM or COG(center of geometry)
algorithm : string, optional
"dynamic" or "static". The static one is slower. I
loops over all atoms and then merges cluster, whereas
the dynamic algorithm grows clusters dynamically.
work_in : string, optional
"Residue" or "Atom". Either work in (and output)
ResidueGroups or AtomGroups.
The former may be faster for systems in which all
parts of the same molecule are always in the same cluster,
whereas the latter is useful for systems in which different
parts of the same molecule can be in different clusters
(i.e. block copolymers).
traj_pbc_style : string, optional
Gromacs pbc definitions: mol or atom, by default
None
pbc : bool, optional
Whether to consider periodic boundary conditions in the
neighbour search (for determining whether atoms belong to
the same cluster), by default True. Note that if work_in is
set to "Residue" periodic boundary conditions are taken into
account implicitly for atoms in molecules passing across the
boundaries.
Raises
------
NotImplementedError
If an unspecified algorithm or work_in is choosen
ValueError
If pbc is not boolean
ToDo
----
-Make static and dynamic algorithms store the same arguments
-Add plotting capabilities
-Add capabilities to only look at certain time windows
-Get rid of traj and coord attributes
"""
self._set_pbc_style(traj_pbc_style)
self.universe = self._get_universe(self._coord, traj=self._traj)
self.style = style
self.aggregate_species = self._select_species(self.universe,
style=self.style)
self.cluster_list = []
# Initialise the neighboursearch object
if pbc == True:
self.neighbour_search = NeighborSearch.AtomNeighborSearch(
self.aggregate_species,
box=self.universe.dimensions,
bucket_size=10)
elif pbc == False:
if work_in == "Residue" and traj_pbc_style != "mol":
warnings.warn('work_in = "Residue" implicitly enforces pbc '\
'for atoms in the same molecule if pbc_style '\
'= "atom"', UserWarning)
print('Warning')
self.neighbour_search = NeighborSearch.AtomNeighborSearch(
self.aggregate_species, box=None, bucket_size=10)
else:
raise ValueError("pbc has to be boolean")
if work_in == "Residue":
self.search_level = "R"
elif work_in == "Atom":
self.search_level = "A"
else:
raise NotImplementedError(
"{:s} is unspecified work_in variable".format(work_in))
if algorithm == "static":
cluster_algorithm = self._get_cluster_list_static
elif algorithm == "dynamic":
cluster_algorithm = self._get_cluster_list_dynamic
else:
raise NotImplementedError(
"{:s} is unspecified algorithm".format(algorithm))
# Loop over all trajectory times
for time in self.universe.trajectory:
if times is not None:
if time.time > max(times) or time.time < min(times):
continue
self.cluster_list.append(cluster_algorithm())
print("****TIME: {:8.2f}".format(time.time))
print("---->Number of clusters {:d}".format(
len(self.cluster_list[-1])))
# Rewind Trajectory to beginning for other analysis
self.universe.trajectory.rewind()
def voronoi_tessel(ts):
# set the time step
print 'Frame %i in %i'%(ts, end_f)
u = MDAnalysis.Universe(top,traj)
u.trajectory[0]
# Select atoms within this particular frame
lpd1_atoms = u.select_atoms(sel1)
lpd2_atoms = u.select_atoms(sel2)
lpd3_atoms = u.select_atoms(sel3)
zmean = np.mean(np.concatenate([lpd1_atoms.positions[:,2], lpd2_atoms.positions[:,2], lpd3_atoms.positions[:,2]]))
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# select atoms in the upper leaflet using positions in the first frame of simulation
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet in the current frame
if side == 'up':
lpd1i=[]
zpos = lpd1_atoms.positions[:,2]
for i in range(num_lpd1):
if zpos[i] > zmean:
lpd1i.append(lpd1_atoms[i])
lpd1i = np.sum(np.array(lpd1i))
lpd2i=[]
zpos = lpd2_atoms.positions[:,2]
for i in range(num_lpd2):
if zpos[i] > zmean:
lpd2i.append(lpd2_atoms[i])
lpd2i = np.sum(np.array(lpd2i))
lipids = lpd1i + lpd2i
u.trajectory[ts] # now move to the frame currently being analyzed
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids,15.0)
elif side == 'down':
lpd1i=[]
zpos = lpd1_atoms.positions[:,2]
for i in range(num_lpd1):
if zpos[i] < zmean:
lpd1i.append(lpd1_atoms[i])
lpd1i = np.sum(np.array(lpd1i))
lpd2i=[]
zpos = lpd2_atoms.positions[:,2]
for i in range(num_lpd2):
if zpos[i] < zmean:
lpd2i.append(lpd2_atoms[i])
lpd2i = np.sum(np.array(lpd2i))
lipids = lpd1i + lpd2i
u.trajectory[ts] # now move to the frame currently being analyzed
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids,15.0)
lpd_atms = lpd1i + lpd2i + lpd3i
#Extracting the coordinates
Pxyz = lpd_atms.positions
Pxy = []
for l in range(0,len(Pxyz)) :
Pxy.append([Pxyz[l][0],Pxyz[l][1]])
#Extracting xy coordinates and residue names
atm_list = []
for a in range(0, len(Pxyz)):
atm_list.append([Pxyz[a][0],Pxyz[a][1],lpd_atms[a].resname])
#Introducing PBC
x_box = u.dimensions[0]
y_box = u.dimensions[1]
xplus = []
xminus = []
xyplus = []
xyminus = []
for atm in range(0 ,len(atm_list)):
xplus.append([atm_list[atm][0]+x_box,atm_list[atm][1],atm_list[atm][2]])
xminus.append([atm_list[atm][0]-x_box,atm_list[atm][1],atm_list[atm][2]])
atm_list_px = atm_list + xplus + xminus
for atm in range(0 ,len(atm_list_px)):
xyplus.append([atm_list_px[atm][0],atm_list_px[atm][1]+y_box,atm_list_px[atm][2]])
xyminus.append([atm_list_px[atm][0],atm_list_px[atm][1]-y_box,atm_list_px[atm][2]])
atm_list_p = atm_list_px + xyplus + xyminus
atm_xy = []
for i in range(0,len(atm_list_p)) :
atm_xy.append([atm_list_p[i][0],atm_list_p[i][1]])
vor = Voronoi(atm_xy)
vor_s = Voronoi(Pxy)
vertices = vor.vertices
ridge_points = vor.ridge_points
Lpd1_Lpd1_I = 0
Lpd2_Lpd2_I = 0
Lpd3_Lpd3_I = 0
Lpd1_Lpd2_I = 0
Lpd1_Lpd3_I = 0
Lpd2_Lpd3_I = 0
Lpd1_Lpd1_E = 0
Lpd2_Lpd2_E = 0
Lpd3_Lpd3_E = 0
Lpd1_Lpd2_E = 0
Lpd1_Lpd3_E = 0
Lpd2_Lpd3_E = 0
r_length = len(ridge_points)
for k in range (0,r_length) :
ridge_k = ridge_points[k]
Li = atm_list_p[int(ridge_k[0])]
Lj = atm_list_p[int(ridge_k[1])]
#Lipids INSIDE the box
if 0 < Li[0] < x_box and 0 < Li[1] < y_box and 0 < Lj[0] < x_box and 0 < Lj[1] < y_box :
if Li[2] == lipid1 and Lj[2] == lipid1:
Lpd1_Lpd1_I = Lpd1_Lpd1_I + 1
if Li[2] == lipid2 and Lj[2] == lipid2:
Lpd2_Lpd2_I = Lpd2_Lpd2_I + 1
if Li[2] == lipid3 and Lj[2] == lipid3:
Lpd3_Lpd3_I = Lpd3_Lpd3_I + 1
if Li[2] == lipid1 and Lj[2] == lipid2:
Lpd1_Lpd2_I = Lpd1_Lpd2_I + 1
if Li[2] == lipid2 and Lj[2] == lipid1:
Lpd1_Lpd2_I = Lpd1_Lpd2_I + 1
if Li[2] == lipid1 and Lj[2] == lipid3:
Lpd1_Lpd3_I = Lpd1_Lpd3_I + 1
if Li[2] == lipid3 and Lj[2] == lipid1:
Lpd1_Lpd3_I = Lpd1_Lpd3_I + 1
if Li[2] == lipid2 and Lj[2] == lipid3:
Lpd2_Lpd3_I = Lpd2_Lpd3_I + 1
if Li[2] == lipid3 and Lj[2] == lipid2:
Lpd2_Lpd3_I = Lpd2_Lpd3_I + 1
#Lipids at the EDGE of the box
if 0 <= Li[0] < x_box and 0 <= Li[1] < y_box or 0 <= Lj[0] < x_box and 0 <= Lj[1] < y_box :
if Li[2] == lipid1 and Lj[2] == lipid1:
Lpd1_Lpd1_E = Lpd1_Lpd1_E + 1
if Li[2] == lipid2 and Lj[2] == lipid2:
Lpd2_Lpd2_E = Lpd2_Lpd2_E + 1
if Li[2] == lipid3 and Lj[2] == lipid3:
Lpd3_Lpd3_E = Lpd3_Lpd3_E + 1
if Li[2] == lipid1 and Lj[2] == lipid2:
Lpd1_Lpd2_E = Lpd1_Lpd2_E + 1
if Li[2] == lipid2 and Lj[2] == lipid1:
Lpd1_Lpd2_E = Lpd1_Lpd2_E + 1
if Li[2] == lipid1 and Lj[2] == lipid3:
Lpd1_Lpd3_E = Lpd1_Lpd3_E + 1
if Li[2] == lipid3 and Lj[2] == lipid1:
Lpd1_Lpd3_E = Lpd1_Lpd3_E + 1
if Li[2] == lipid2 and Lj[2] == lipid3:
Lpd2_Lpd3_E = Lpd2_Lpd3_E + 1
if Li[2] == lipid3 and Lj[2] == lipid2:
Lpd2_Lpd3_E = Lpd2_Lpd3_E + 1
#Total = LipidsInside + (Lipids including EDGES - Lipids Inside)/2 -----> Correction for over counting the lipids in periodic images
Lpd1_Lpd1 = Lpd1_Lpd1_I + (Lpd1_Lpd1_E - Lpd1_Lpd1_I)/2
Lpd2_Lpd2 = Lpd2_Lpd2_I + (Lpd2_Lpd2_E - Lpd2_Lpd2_I)/2
Lpd3_Lpd3 = Lpd3_Lpd3_I + (Lpd3_Lpd3_E - Lpd3_Lpd3_I)/2
Lpd1_Lpd2 = Lpd1_Lpd2_I + (Lpd1_Lpd2_E - Lpd1_Lpd2_I)/2
Lpd1_Lpd3 = Lpd1_Lpd3_I + (Lpd1_Lpd3_E - Lpd1_Lpd3_I)/2
Lpd2_Lpd3 = Lpd2_Lpd3_I + (Lpd2_Lpd3_E - Lpd2_Lpd3_I)/2
sum_bonds = Lpd1_Lpd1 + Lpd2_Lpd2 + Lpd3_Lpd3 + Lpd1_Lpd2 + Lpd1_Lpd3 + Lpd2_Lpd3
#Considering only Similar Lipid (SL) and Dissimilar Lipid (DL) Bonds
SL = Lpd1_Lpd1 + Lpd2_Lpd2 + Lpd3_Lpd3
DL = Lpd1_Lpd2 + Lpd1_Lpd3 + Lpd2_Lpd3
#Calculating Fractions
X_SL = float(SL)/float(sum_bonds) #Similar Lipid
X_DL = float(DL)/float(sum_bonds) #Dissimilar Lipid
#Mixing Entropy
mix_entropy = -(X_SL * np.log2(X_SL)) +( X_DL * np.log2(X_DL))
#Calculating Averages
sum_bonds = Lpd1_Lpd1 + Lpd1_Lpd2 + Lpd2_Lpd2
avg_bonds = float(sum_bonds)/float(len(atm_list))
return Lpd1_Lpd1, Lpd2_Lpd2, Lpd3_Lpd3, Lpd1_Lpd2, Lpd1_Lpd3, Lpd2_Lpd3, sum_bonds, avg_bonds, mix_entropy
def extract_data(frame):
#for frame in frames:
u = MDAnalysis.Universe(psf, trr)
print 'Frame %i of %i......' % (frame, u.trajectory.n_frames)
u.trajectory[frame]
XBOX = u.dimensions[0]
YBOX = u.dimensions[1]
##################################################################################
### Determining side of the bilayer CHOL belongs to in this frame
#Lipid Residue names
lpd1_atoms = u.select_atoms(sel1)
lpd2_atoms = u.select_atoms(sel2)
lpd3_atoms = u.select_atoms(sel3)
#Protein atom selction
prot_atoms = u.select_atoms(selprot)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
num_lpd3 = lpd3_atoms.n_atoms
# atoms in the upper leaflet as defined by insane.py or the MARTINI-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
if side == 'up':
lpd1i = lpd1_atoms[:int((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:int((num_lpd2) / 2)]
phospholipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms) #CHOL
lpd3i = ns_lipids.search(phospholipids, 15.0)
#proti = prot_atoms.select_atoms(protsel_up)
elif side == 'down':
lpd1i = lpd1_atoms[int((num_lpd1) / 2):]
lpd2i = lpd2_atoms[int((num_lpd2) / 2):]
phospholipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms) #CHOL
lpd3i = ns_lipids.search(phospholipids, 15.0)
#proti = prot_atoms.select_atoms(protsel_down)
#Using tail definitions
groups1 = []
for i in np.arange(len(lpd1i.resnums)):
resnum = lpd1i.resnums[i]
group = u.select_atoms(
'resname DPPC and resnum %i and (name C2A or name C2B)' % resnum)
groups1.append(group)
lpd1i = np.sum(groups1)
groups2 = []
for i in np.arange(len(lpd2i.resnums)):
resnum = lpd2i.resnums[i]
group = u.select_atoms(
'resname DIPC and resnum %i and (name D2A or name D2B)' % resnum)
groups2.append(group)
lpd2i = np.sum(groups2)
groups3 = []
for i in np.arange(len(lpd3i.resnums)):
resnum = lpd3i.resnums[i]
group = u.select_atoms('resname CHOL and resnum %i and (name R3)' %
resnum)
groups3.append(group)
lpd3i = np.sum(groups3)
if protein == 'YES':
#Selecting Protein atoms that are on the tail plane.
phospholipidtails = lpd1i + lpd2i #Phospholipid tail atoms that defines the plane of interest.
ns_PROT = NS.AtomNeighborSearch(prot_atoms) #Protein
proti = ns_PROT.search(
phospholipidtails, 10.0
) #Protein atoms that are within 1.0nm of the Phospholipid tail atoms.
u_leaflet = lpd1i + lpd2i + lpd3i + proti
else:
u_leaflet = lpd1i + lpd2i + lpd3i
##################################################################################
#Collecting coordinates of the interface atoms
mem_plane = []
mem_plane_composition = []
if protein == 'YES':
for selatm in proti:
mem_plane.append(selatm.position)
mem_plane_composition.append('PROT')
for selatm in lpd1i:
mem_plane.append(selatm.position)
mem_plane_composition.append(lipid1)
for selatm in lpd2i:
mem_plane.append(selatm.position)
mem_plane_composition.append(lipid2)
for selatm in lpd3i:
mem_plane.append(selatm.position)
mem_plane_composition.append(lipid3)
mem_plane_data = [mem_plane, mem_plane_composition, XBOX, YBOX]
return mem_plane_data
def calcAPL(frame):
print frame
u = MDAnalysis.Universe(psf, trr)
u.trajectory[frame]
#Lipid Residue names
lpd1_atoms = u.select_atoms('resname %s and name PO4' % lipid1)
lpd2_atoms = u.select_atoms('resname %s and name PO4' % lipid2)
lpd3_atoms = u.select_atoms('resname %s and name ROH' % lipid3)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
#Separating upper and lower leaflets
# atoms in the upper leaflet as defined by insane.py or the CHARMM-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
if side == 'up':
lpd1i = lpd1_atoms[:((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:((num_lpd2) / 2)]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
elif side == 'down':
lpd1i = lpd1_atoms[((num_lpd1) / 2):]
lpd2i = lpd2_atoms[((num_lpd2) / 2):]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
lpd_atms = lpd1i + lpd2i + lpd3i
nlipid = lpd_atms.n_atoms
frm_l1_lpd_area = []
frm_l2_lpd_area = []
frm_l3_lpd_area = []
#Extracting the coordinates
Pxyz = lpd_atms.positions
Pxy = []
for l in range(0, len(Pxyz)):
Pxy.append([Pxyz[l][0], Pxyz[l][1]])
#Extracting xy coordinates and residue names
atmlist = []
for a in range(0, len(Pxyz)):
atmlist.append([Pxyz[a][0], Pxyz[a][1], lpd_atms[a].resname])
xbox = u.dimensions[0]
ybox = u.dimensions[1]
atm_list_pbc = introducePBC(xbox, ybox, atmlist)
atm_xy = []
for i in range(0, len(atm_list_pbc)):
atm_xy.append([atm_list_pbc[i][0], atm_list_pbc[i][1]])
vor = Voronoi(atm_xy)
vor_s = Voronoi(Pxy)
vertices = vor.vertices
#Selecting the Index of the Voronoi region for each input point in siede the box
point_region_box = vor.point_region[:nlipid]
point_region_pbc = vor.point_region
for k in range(len(point_region_box)):
point_region_k = point_region_box[k]
vor_vert = vor.regions[point_region_k]
vor_vert_coor = calcVerticeCoordinates(vor_vert, vor)
lpd_area = calcAreaofPolygon(vor_vert_coor)
if atm_list_pbc[k][2] == lipid1:
frm_l1_lpd_area.append(lpd_area)
elif atm_list_pbc[k][2] == lipid2:
frm_l2_lpd_area.append(lpd_area)
elif atm_list_pbc[k][2] == lipid3:
frm_l3_lpd_area.append(lpd_area)
else:
frm_GM_lpd_area.append(lpd_area)
return frm_l1_lpd_area, frm_l2_lpd_area, frm_l3_lpd_area, frm_GM_lpd_area
def get_side_coordinates_and_box(u, time_ts):
"""Assign lipids to leaflets, retrieve their coordinates, resIDs and the director order parameter u=3/2cosˆ2(theta)-1/2"""
x, y, z = u.trajectory.ts.triclinic_dimensions[0][
0], u.trajectory.ts.triclinic_dimensions[1][
1], u.trajectory.ts.triclinic_dimensions[2][2]
box = np.array([x, y, z])
### Determining side of the bilayer CHOL belongs to in this frame
#Lipid Residue names
lipid1 = 'DSPC'
#lipid2 ='DAPC'
lipid2 = 'DLIP'
lipid3 = 'CHL'
lpd1_atoms = u.select_atoms('resname %s and name P' % lipid1)
lpd2_atoms = u.select_atoms('resname %s and name P' % lipid2)
lpd3_atoms = u.select_atoms('resname %s and name O2' % lipid3)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# atoms in the upper leaflet as defined by insane.py or the CHARMM-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
# this must be done because CHOL rapidly flip-flops between leaflets in the MARTINI model
# so we must assign CHOL to each leaflet at every time step, and in large systems
# with substantial membrane undulations, a simple cut-off in the z-axis just will not cut it
if side == 'up':
lpd1i = lpd1_atoms[:int((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:int((num_lpd2) / 2)]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
elif side == 'down':
lpd1i = lpd1_atoms[int((num_lpd1) / 2):]
lpd2i = lpd2_atoms[int((num_lpd2) / 2):]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
#define the cholesterol
# ID center of geometry coordinates for cholesterol on indicated bilayer side
#print(lpd3i)
lpd3_coords = np.zeros((len(lpd3i.resnums), 3))
lpd3_res = np.zeros((len(lpd3i.resnums), 1))
lpd3_u = np.zeros((len(lpd3i.resnums), 1))
for i in np.arange(len(lpd3i.resnums)):
resnum = lpd3i.resnums[i]
head_CHL = u.select_atoms('resnum %i and (name C1)' %
resnum).center_of_geometry()
tail_CHL = u.select_atoms('resnum %i and (name C65)' %
resnum).center_of_geometry()
vect_CHL = head_CHL - tail_CHL
theta_CHL = np.arccos(
np.dot(vect_CHL, vref) / (norm(vect_CHL) * norm(vref)))
u_CHL = 1.5 * ((pow(np.cos(theta_CHL), 2))) - 0.5
group = u.select_atoms('resnum %i' % resnum)
group_cog = group.center_of_geometry()
lpd3_coords[i] = group_cog
lpd3_res[i] = resnum
lpd3_u[i] = u_CHL
# ID coordinates for lipids on indicated bilayer side, renaming variables
lpd1_coordsA = np.zeros((len(lpd1i.resnums), 3))
lpd1_coordsB = np.zeros((len(lpd1i.resnums), 3))
lpd1_res = np.zeros((len(lpd1i.resnums), 1))
lpd1_u = np.zeros((len(lpd1i.resnums), 1))
for i in np.arange(len(lpd1i.resnums)):
resnum_A = lpd1i.resnums[i]
resnum_B = lpd1i.resnums[i]
###test the lipids-end-tails
head_DSPC_A = u.select_atoms('resnum %i and (name C22)' %
resnum_A).center_of_geometry()
tail_DSPC_A = u.select_atoms('resnum %i and (name 6C21)' %
resnum_A).center_of_geometry()
vect_DSPC_A = head_DSPC_A - tail_DSPC_A
theta_DSPC_A = np.arccos(
np.dot(vect_DSPC_A, vref) / (norm(vect_DSPC_A) * norm(vref)))
head_DSPC_B = u.select_atoms('resnum %i and (name C32)' %
resnum_B).center_of_geometry()
tail_DSPC_B = u.select_atoms('resnum %i and (name 6C31)' %
resnum_B).center_of_geometry()
vect_DSPC_B = head_DSPC_B - tail_DSPC_B
theta_DSPC_B = np.arccos(
np.dot(vect_DSPC_B, vref) / (norm(vect_DSPC_B) * norm(vref)))
theta_DSPC = (theta_DSPC_A + theta_DSPC_B) / 2
u_DSPC = ((3 / 2) * (pow(np.cos(theta_DSPC), 2))) - 0.5
#print(u_DPPC)
lpd1_u[i] = u_DSPC
group_lpd1_chainA = u.select_atoms(
'resnum %i and (name C26 or name C27 or name C28 or name C29 )' %
resnum_A)
group_lpd1_chainB = u.select_atoms(
'resnum %i and (name C36 or name C37 or name C38 or name C39)' %
resnum_B)
group_cog_lpd1A = group_lpd1_chainA.center_of_geometry()
group_cog_lpd1B = group_lpd1_chainB.center_of_geometry()
lpd1_coordsA[i] = group_cog_lpd1A
lpd1_coordsB[i] = group_cog_lpd1B
lpd1_res[i] = resnum_A
lpd2_coordsA = np.zeros((len(lpd2i.resnums), 3))
lpd2_coordsB = np.zeros((len(lpd2i.resnums), 3))
lpd2_res = np.zeros((len(lpd2i.resnums), 1))
lpd2_u = np.zeros((len(lpd2i.resnums), 1))
for i in np.arange(len(lpd2i.resnums)):
resnumB_A = lpd2i.resnums[i]
resnumB_B = lpd2i.resnums[i]
#head_DAPC_A = u.select_atoms('resnum %i and (name C24)'%resnumB_A).center_of_geometry()
#tail_DAPC_A = u.select_atoms('resnum %i and (name 6C21)'%resnumB_A).center_of_geometry()
#head_DLIP_A = u.select_atoms('resnum %i and (name C24)'%resnumB_A).center_of_geometry()
#print(head_DLIP_A)
head_DLIP_A = u.select_atoms(
'resnum %i and (name C24)' %
resnumB_A).positions #changed for positions
tail_DLIP_A = u.select_atoms('resnum %i and (name 6C21)' %
resnumB_A).center_of_geometry()
#print(pos_DLIP_A)
# vect_DAPC_A = head_DAPC_A - tail_DAPC_A
# theta_DAPC_A = np.arccos(np.dot(vect_DAPC_A, vref)/(norm(vect_DAPC_A)*norm(vref)))
vect_DLIP_A = head_DLIP_A - tail_DLIP_A
theta_DLIP_A = np.arccos(
np.dot(vect_DLIP_A, vref) / (norm(vect_DLIP_A) * norm(vref)))
# head_DAPC_B = u.select_atoms('resnum %i and (name C34)'%resnumB_B).center_of_geometry()
# tail_DAPC_B = u.select_atoms('resnum %i and (name 6C31)'%resnumB_B).center_of_geometry()
head_DLIP_B = u.select_atoms('resnum %i and (name C34)' %
resnumB_B).center_of_geometry()
tail_DLIP_B = u.select_atoms('resnum %i and (name 6C31)' %
resnumB_B).center_of_geometry()
# vect_DAPC_B = head_DAPC_B - tail_DAPC_B
# theta_DAPC_B = np.arccos(np.dot(vect_DAPC_B, vref)/(norm(vect_DAPC_B)*norm(vref)))
# theta_DAPC = (theta_DAPC_A + theta_DAPC_B)/2
vect_DLIP_B = head_DLIP_B - tail_DLIP_B
theta_DLIP_B = np.arccos(
np.dot(vect_DLIP_B, vref) / (norm(vect_DLIP_B) * norm(vref)))
theta_DLIP = (theta_DLIP_A + theta_DLIP_B) / 2
# u_DAPC= ((3/2)*(pow(np.cos(theta_DAPC), 2))) - 0.5
# lpd2_u[i] = u_DAPC
u_DLIP = ((3 / 2) * (pow(np.cos(theta_DLIP), 2))) - 0.5
lpd2_u[i] = u_DLIP
group_lpd2_chainA = u.select_atoms(
'resnum %i and (name C26 or name C27 or name C28 or name C29)' %
resnumB_A)
group_lpd2_chainB = u.select_atoms(
'resnum %i and (name C36 or name C37 or name C38 or name C39)' %
resnumB_B)
group_cog_lpd2A = group_lpd2_chainA.center_of_geometry()
lpd2_coordsA[i] = group_cog_lpd2A
group_cog_lpd2B = group_lpd2_chainB.center_of_geometry()
lpd2_coordsB[i] = group_cog_lpd2B
lpd2_res[i] = resnumB_A
lpd_coords = np.vstack((lpd1_coordsA, lpd1_coordsB, lpd2_coordsA,
lpd2_coordsB, lpd3_coords)) #append
lpd_resids = np.vstack((lpd1_res, lpd1_res, lpd2_res, lpd2_res, lpd3_res))
lpd_us = np.vstack((lpd1_u, lpd1_u, lpd2_u, lpd2_u, lpd3_u))
#print(time_ts)
file = open("testfile.txt", "a")
file.write(str(time_ts.frame) + "\n")
file.close()
return lpd_coords, lpd_resids, lpd_us, box
def get_side_coordinates_and_box(frame):
u = MDAnalysis.Universe(top, traj)
u.trajectory[frame]
x, y, z = u.trajectory.ts.triclinic_dimensions[0][
0], u.trajectory.ts.triclinic_dimensions[1][
1], u.trajectory.ts.triclinic_dimensions[2][2]
box = np.array([x, y, z])
### Determining side of the bilayer CHOL belongs to in this frame
#Lipid Residue names
lipid1 = 'DPPC'
lipid2 = 'DFPC'
lipid3 = 'CHOL'
lpd1_atoms = u.select_atoms('resname %s and name PO4' % lipid1)
lpd2_atoms = u.select_atoms('resname %s and name PO4' % lipid2)
lpd3_atoms = u.select_atoms('resname %s and name ROH' % lipid3)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# atoms in the upper leaflet as defined by insane.py or the CHARMM-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
# this must be done because CHOL rapidly flip-flops between leaflets in the MARTINI model
# so we must assign CHOL to each leaflet at every time step, and in large systems
# with substantial membrane undulations, a simple cut-off in the z-axis just will not cut it
if side == 'up':
lpd1i = lpd1_atoms[:((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:((num_lpd2) / 2)]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
elif side == 'down':
lpd1i = lpd1_atoms[((num_lpd1) / 2):]
lpd2i = lpd2_atoms[((num_lpd2) / 2):]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
# ID center of geometry coordinates for cholesterol on indicated bilayer side
lpd3_coords = np.zeros((len(lpd3i.resnums), 3))
for i in np.arange(len(lpd3i.resnums)):
resnum = lpd3i.resnums[i]
group = u.select_atoms(
'resnum %i and (name R1 or name R2 or name R3 or name R4 or name R5)'
% resnum)
group_cog = group.center_of_geometry()
lpd3_coords[i] = group_cog
# ID coordinates for lipids on indicated bilayer side, renaming variables
lpd1_atoms = u.select_atoms('resname %s and (name C2A or name C2B)' %
lipid1)
lpd2_atoms = u.select_atoms('resname %s and (name D2A or name D2B)' %
lipid2)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
# select lipid tail atoms beloging to the selected bilayer side
if side == 'up':
lpd1i = lpd1_atoms[:((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:((num_lpd2) / 2)]
elif side == 'down':
lpd1i = lpd1_atoms[((num_lpd1) / 2):]
lpd2i = lpd2_atoms[((num_lpd2) / 2):]
# assign lpd1 and lpd2 coordinates, completing the assignment of all coordinates from which psi6 will be computed
lpd1_coords = lpd1i.positions
lpd2_coords = lpd2i.positions
#lpd_coords = np.vstack((lpd1_coords,lpd2_coords,lpd3_coords))
#lpd_coords = np.vstack((lpd1_coords,lpd2_coords,lpd3_coords))
lpd_coords = np.vstack((lpd1_coords, lpd3_coords))
lpd_coords = lpd_coords.astype('float32')
return lpd_coords, box
def voronoi_tessel(frame):
# set the time step
print 'Frame %i in %i' % (frame, end_f)
u = MDAnalysis.Universe(psf, trr)
u.trajectory[int(frame)]
# Select atoms within this particular frame
lpd1_atoms = u.select_atoms('resname %s and name PO4' % lipid1)
lpd2_atoms = u.select_atoms('resname %s and name PO4' % lipid2)
lpd3_atoms = u.select_atoms('resname %s and name ROH' % lipid3)
prot_atoms = u.select_atoms(selprot)
num_lpd1 = lpd1_atoms.n_atoms
num_lpd2 = lpd2_atoms.n_atoms
#Separating upper and lower leaflets
# atoms in the upper leaflet as defined by insane.py or the CHARMM-GUI membrane builders
# select cholesterol headgroups within 1.5 nm of lipid headgroups in the selected leaflet
if side == 'up':
lpd1i = lpd1_atoms[:((num_lpd1) / 2)]
lpd2i = lpd2_atoms[:((num_lpd2) / 2)]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
elif side == 'down':
lpd1i = lpd1_atoms[((num_lpd1) / 2):]
lpd2i = lpd2_atoms[((num_lpd2) / 2):]
lipids = lpd1i + lpd2i
ns_lipids = NS.AtomNeighborSearch(lpd3_atoms)
lpd3i = ns_lipids.search(lipids, 15.0)
if plane_of_interest == 'TAIL':
#Using tail definitions
groups1 = []
for i in np.arange(len(lpd1i.resnums)):
resnum = lpd1i.resnums[i]
group = u.select_atoms(
'resname %s and resnum %i and (name C2A or name C2B)' %
(lipid1, resnum))
groups1.append(group)
lpd1i = np.sum(groups1)
groups2 = []
for i in np.arange(len(lpd2i.resnums)):
resnum = lpd2i.resnums[i]
group = u.select_atoms(
'resname %s and resnum %i and (name D2A or name D2B)' %
(lipid2, resnum))
groups2.append(group)
lpd2i = np.sum(groups2)
groups3 = []
for i in np.arange(len(lpd3i.resnums)):
resnum = lpd3i.resnums[i]
group = u.select_atoms('resname CHOL and resnum %i and (name R3)' %
resnum)
groups3.append(group)
lpd3i = np.sum(groups3)
if protein == 'YES':
#Selecting Protein atoms that are on the membrane plane.
phospholipidgrid = lpd1i + lpd2i #Phospholipid tail atoms that defines the plane of interest.
ns_PROT = NS.AtomNeighborSearch(prot_atoms) #Protein
proti = ns_PROT.search(
phospholipidgrid,
10.0) #Protein atoms that are within 1.0nm of the membrane
u_leaflet = lpd1i + lpd2i + lpd3i + proti
else:
u_leaflet = lpd1i + lpd2i + lpd3i
#Extracting the coordinates
lpd_atms = u_leaflet
Pxyz = lpd_atms.positions
Pxy = []
for l in range(0, len(Pxyz)):
Pxy.append([Pxyz[l][0], Pxyz[l][1]])
#Extracting xy coordinates and residue names
atm_list = []
for a in range(0, len(Pxyz)):
#print lpd_atms[a].resname
atm_list.append(
[Pxyz[a][0], Pxyz[a][1], lpd_atms[a].resname, lpd_atms[a].segid])
#Introducing PBC
x_box = u.dimensions[0]
y_box = u.dimensions[1]
xplus = []
xminus = []
xyplus = []
xyminus = []
for atm in range(0, len(atm_list)):
xplus.append([
atm_list[atm][0] + x_box, atm_list[atm][1], atm_list[atm][2],
atm_list[atm][3]
])
xminus.append([
atm_list[atm][0] - x_box, atm_list[atm][1], atm_list[atm][2],
atm_list[atm][3]
])
atm_list_px = atm_list + xplus + xminus
for atm in range(0, len(atm_list_px)):
xyplus.append([
atm_list_px[atm][0], atm_list_px[atm][1] + y_box,
atm_list_px[atm][2], atm_list_px[atm][3]
])
xyminus.append([
atm_list_px[atm][0], atm_list_px[atm][1] - y_box,
atm_list_px[atm][2], atm_list_px[atm][3]
])
atm_list_p = atm_list_px + xyplus + xyminus
atm_xy = []
for i in range(0, len(atm_list_p)):
atm_xy.append([atm_list_p[i][0], atm_list_p[i][1]])
vor = Voronoi(atm_xy)
vor_s = Voronoi(Pxy)
vertices = vor.vertices
ridge_points = vor.ridge_points
#Plotting Voroni Diagrams
vor_rgns = vor.regions
l_vor_rgns = len(vor_rgns)
vor_points = vor.point_region
l_vor_points = len(vor_points)
if PRINT_VOR == 'YES' and np.mod(frame, PRINT_FREQ) == 0:
plt.clf()
#voronoi_plot_2d(vor_s)
for p in range(0, l_vor_points):
rgn = vor_rgns[vor_points[p]]
L = atm_list_p[p]
if not -1 in rgn and 0 <= L[0] < x_box and 0 <= L[1] < y_box:
if L[2] == lipid1:
polygon = [vor.vertices[i] for i in rgn]
plt.plot(*zip(*polygon), color='black')
plt.fill(*zip(*polygon), color='blue')
elif L[2] == lipid2:
polygon = [vor.vertices[i] for i in rgn]
plt.plot(*zip(*polygon), color='black')
plt.fill(*zip(*polygon), color='red')
elif L[2] == lipid3:
polygon = [vor.vertices[i] for i in rgn]
plt.plot(*zip(*polygon), color='black')
plt.fill(*zip(*polygon), color='green')
else:
polygon = [vor.vertices[i] for i in rgn]
plt.plot(*zip(*polygon), color='black')
plt.fill(*zip(*polygon), color=PROT_color)
plt.axis('equal')
if side == 'up':
plt.savefig('VT/img' + str('%03d' % frame) + '.up.png')
if side == 'down':
plt.savefig('VT/img' + str('%03d' % frame) + '.down.png')
Lpd1_Lpd1_I = 0
Lpd2_Lpd2_I = 0
Lpd3_Lpd3_I = 0
Lpd1_Lpd2_I = 0
Lpd1_Lpd3_I = 0
Lpd2_Lpd3_I = 0
Lpd1_Lpd1_E = 0
Lpd2_Lpd2_E = 0
Lpd3_Lpd3_E = 0
Lpd1_Lpd2_E = 0
Lpd1_Lpd3_E = 0
Lpd2_Lpd3_E = 0
Prot_Lpd1_I = 0
Prot_Lpd2_I = 0
Prot_Lpd3_I = 0
Prot_Prot_I = 0
Prot_Lpd1_E = 0
Prot_Lpd2_E = 0
Prot_Lpd3_E = 0
Prot_Prot_E = 0
r_length = len(ridge_points)
for k in range(0, r_length):
ridge_k = ridge_points[k]
Li = atm_list_p[int(ridge_k[0])]
Lj = atm_list_p[int(ridge_k[1])]
#print 'Li', Li[3], Li[2]
#print 'Lj', Lj[3], Lj[2]
#Lipids INSIDE the box
if 0 < Li[0] < x_box and 0 < Li[1] < y_box and 0 < Lj[
0] < x_box and 0 < Lj[1] < y_box:
#Lipid Lipid contacts
if Li[2] == lipid1 and Lj[2] == lipid1:
Lpd1_Lpd1_I = Lpd1_Lpd1_I + 1
if Li[2] == lipid2 and Lj[2] == lipid2:
Lpd2_Lpd2_I = Lpd2_Lpd2_I + 1
if Li[2] == lipid3 and Lj[2] == lipid3:
Lpd3_Lpd3_I = Lpd3_Lpd3_I + 1
if Li[2] == lipid1 and Lj[2] == lipid2:
Lpd1_Lpd2_I = Lpd1_Lpd2_I + 1
if Li[2] == lipid2 and Lj[2] == lipid1:
Lpd1_Lpd2_I = Lpd1_Lpd2_I + 1
if Li[2] == lipid1 and Lj[2] == lipid3:
Lpd1_Lpd3_I = Lpd1_Lpd3_I + 1
if Li[2] == lipid3 and Lj[2] == lipid1:
Lpd1_Lpd3_I = Lpd1_Lpd3_I + 1
if Li[2] == lipid2 and Lj[2] == lipid3:
Lpd2_Lpd3_I = Lpd2_Lpd3_I + 1
if Li[2] == lipid3 and Lj[2] == lipid2:
Lpd2_Lpd3_I = Lpd2_Lpd3_I + 1
#Protein lipid contacts
if Li[3] in PROT_seg and Lj[2] == lipid1:
Prot_Lpd1_I = Prot_Lpd1_I + 1
if Li[2] == lipid1 and Lj[3] in PROT_seg:
Prot_Lpd1_I = Prot_Lpd1_I + 1
if Li[3] in PROT_seg and Lj[2] == lipid2:
Prot_Lpd2_I = Prot_Lpd2_I + 1
if Li[2] == lipid2 and Lj[3] in PROT_seg:
Prot_Lpd2_I = Prot_Lpd2_I + 1
if Li[3] in PROT_seg and Lj[2] == lipid3:
Prot_Lpd3_I = Prot_Lpd3_I + 1
if Li[2] == lipid3 and Lj[3] in PROT_seg:
Prot_Lpd3_I = Prot_Lpd3_I + 1
if Li[3] in PROT_seg and Lj[
3] in PROT_seg and Li[3] != Lj[3]: # Avoid self counts
Prot_Prot_I = Prot_Prot_I + 1
#Lipids at the EDGE of the box
#Lipid Lipid contacts
if 0 <= Li[0] < x_box and 0 <= Li[1] < y_box or 0 <= Lj[
0] < x_box and 0 <= Lj[1] < y_box:
if Li[2] == lipid1 and Lj[2] == lipid1:
Lpd1_Lpd1_E = Lpd1_Lpd1_E + 1
if Li[2] == lipid2 and Lj[2] == lipid2:
Lpd2_Lpd2_E = Lpd2_Lpd2_E + 1
if Li[2] == lipid3 and Lj[2] == lipid3:
Lpd3_Lpd3_E = Lpd3_Lpd3_E + 1
if Li[2] == lipid1 and Lj[2] == lipid2:
Lpd1_Lpd2_E = Lpd1_Lpd2_E + 1
if Li[2] == lipid2 and Lj[2] == lipid1:
Lpd1_Lpd2_E = Lpd1_Lpd2_E + 1
if Li[2] == lipid1 and Lj[2] == lipid3:
Lpd1_Lpd3_E = Lpd1_Lpd3_E + 1
if Li[2] == lipid3 and Lj[2] == lipid1:
Lpd1_Lpd3_E = Lpd1_Lpd3_E + 1
if Li[2] == lipid2 and Lj[2] == lipid3:
Lpd2_Lpd3_E = Lpd2_Lpd3_E + 1
if Li[2] == lipid3 and Lj[2] == lipid2:
Lpd2_Lpd3_E = Lpd2_Lpd3_E + 1
#Protein lipid contacts
if Li[3] in PROT_seg and Lj[2] == lipid1:
Prot_Lpd1_E = Prot_Lpd1_E + 1
if Li[2] == lipid1 and Lj[3] in PROT_seg:
Prot_Lpd1_E = Prot_Lpd1_E + 1
if Li[3] in PROT_seg and Lj[2] == lipid2:
Prot_Lpd2_E = Prot_Lpd2_E + 1
if Li[2] == lipid2 and Lj[3] in PROT_seg:
Prot_Lpd2_E = Prot_Lpd2_E + 1
if Li[3] in PROT_seg and Lj[2] == lipid3:
Prot_Lpd3_E = Prot_Lpd3_E + 1
if Li[2] == lipid3 and Lj[3] in PROT_seg:
Prot_Lpd3_E = Prot_Lpd3_E + 1
if Li[3] in PROT_seg and Lj[
3] in PROT_seg and Li[3] != Lj[3]: # Avoid self counts
Prot_Prot_E = Prot_Prot_E + 1
#Total = LipidsInside + (Lipids including EDGES - Lipids Inside)/2 -----> Correction for over counting the lipids in periodic images
Lpd1_Lpd1 = Lpd1_Lpd1_I + (Lpd1_Lpd1_E - Lpd1_Lpd1_I) / 2
Lpd2_Lpd2 = Lpd2_Lpd2_I + (Lpd2_Lpd2_E - Lpd2_Lpd2_I) / 2
Lpd3_Lpd3 = Lpd3_Lpd3_I + (Lpd3_Lpd3_E - Lpd3_Lpd3_I) / 2
Lpd1_Lpd2 = Lpd1_Lpd2_I + (Lpd1_Lpd2_E - Lpd1_Lpd2_I) / 2
Lpd1_Lpd3 = Lpd1_Lpd3_I + (Lpd1_Lpd3_E - Lpd1_Lpd3_I) / 2
Lpd2_Lpd3 = Lpd2_Lpd3_I + (Lpd2_Lpd3_E - Lpd2_Lpd3_I) / 2
Prot_Lpd1 = Prot_Lpd1_I + (Prot_Lpd1_E - Prot_Lpd1_I) / 2
Prot_Lpd2 = Prot_Lpd2_I + (Prot_Lpd2_E - Prot_Lpd2_I) / 2
Prot_Lpd3 = Prot_Lpd3_I + (Prot_Lpd3_E - Prot_Lpd3_I) / 2
Prot_Prot = Prot_Prot_I + (Prot_Prot_E - Prot_Prot_I) / 2
return Lpd1_Lpd1, Lpd2_Lpd2, Lpd3_Lpd3, Lpd1_Lpd2, Lpd1_Lpd3, Lpd2_Lpd3, Prot_Lpd1, Prot_Lpd2, Prot_Lpd3, Prot_Prot
