def cal_SASA(input_pdb, output_prefix):
print "pdb inputs = " + input_pdb
print "output prefix = " + output_prefix
model = openModels.open(input_pdb)
runCommand("surf :all")
out = open(output_prefix + "sasa.txt", "w")
x = '---------------------------------------------------------------------------------\n'
print "list " + str(list(model))
for m in openModels.list(modelTypes=[Molecule]):
msas = 0
for r in m.residues:
try:
sas = r.areaSAS
except AttributeError:
continue
msas = msas + sas
out.write('%s,%f\n' % (r, sas))
out.write(x)
out.write('%s,%f\n' % (m, msas))
out.write('\n')
out.close()
runCommand("del")
print msas
return msas
def main(mask='*.zip', output_directory='.'):
try:
os.mkdir(output_directory)
except:
pass
tan_color = chimera.colorTable.getColorByName('tan')
files = sorted(glob(mask), reverse=True)
# distances = []
# print('Presorting...')
# for i, zip_file in enumerate(files):
# centers = []
# for molecule in parse_zip(zip_file):
# centers.append(center_of_mass(molecule.atoms))
# distances.append(chimera.Point(*centers[0]).distance(chimera.Point(*centers[1])))
# chimera.closeSession()
# distance_sorted = [f for (d, f) in sorted(zip(distances, files), reverse=True)]
for i, zip_file in enumerate(files):
print('{}/{} Rendering {}...'.format(i + 1, len(files), zip_file))
molecules = list(parse_zip(zip_file))
protein = sorted(molecules, key=lambda m: m.numAtoms)[-1]
protein.color = tan_color
if not i:
chimera.runCommand('focus')
render(counter=i, output_dir=output_directory)
chimera.closeSession()
def main():
print sys.argv
if len(sys.argv) != 3: # if no input
print "ERROR: Wrong number of inputs"
print "syntax: chimera --nogui --script \"chimera_move_pdb.py pdbinput output_prefix\""
print len(sys.argv)
return
input_pdb = sys.argv[1]
output_prefix = sys.argv[2]
print "pdb input = " + input_pdb
print "output prefix = "+ output_prefix
model = openModels.open(input_pdb)
#prep(model)
start = 0.0
#list = [start]
for i in range(10):
start = start + 0.03
#list.append(start)
runCommand("move x 0.03 ")
print output_prefix+"."+str(start)+".pdb"
runCommand("write 0 "+output_prefix+"."+str(start)+".pdb")
def recordAnimation(self,
startFrame=None,
endFrame=None,
step=1,
recordArgs="",
encodeArgs=""):
if startFrame is None:
startFrame = self.startFrame
if endFrame is None:
endFrame = self.endFrame
if self.recording:
self.status("Already recording an animation", color="red")
return
self.stopMovieCallback()
self.currentFrame.set(startFrame)
self.recordEnd = endFrame
self.recordStep = step
self.encodeArgs = encodeArgs
self.LoadFrame()
self.recording = True
from chimera import runCommand
self.status("Recording animation...", blankAfter=0)
runCommand("movie record " + recordArgs)
chimera.triggers.addHandler("post-frame", self._startAnimation, None)
def recordAnimation(self, startFrame=None, endFrame=None,
step=1, recordArgs="", encodeArgs=""):
if startFrame is None:
startFrame = self.startFrame
if endFrame is None:
endFrame = self.endFrame
if self.recording:
self.status("Already recording an animation",
color="red")
return
self.stopMovieCallback()
self.currentFrame.set(startFrame)
self.recordEnd = endFrame
self.recordStep = step
self.encodeArgs = encodeArgs
self.LoadFrame()
self.recording = True
from chimera import runCommand
self.status("Recording animation...", blankAfter=0)
runCommand("movie record " + recordArgs)
chimera.triggers.addHandler("post-frame", self._startAnimation,
None)
def abortRecording(self):
if not self.recording:
return
from chimera import runCommand
self.recording = False
runCommand("movie stop; movie reset")
self.status("Animation recording aborted")
def plotPosition(coordinates_file):
with open(coordinates_file, 'r') as cf:
names = {}
points = []
reference = cf.readline().strip()
for line in cf:
name = line.split()[0]
coordinates = line.split()[1:]
if name not in names:
names[name] = len(names)
points.append((coordinates, names[name], name))
color_map = cm.jet
categories = len(names)
if categories == 1:
categories += 1
for point in points:
sphere_shape(radius=0.5,
divisions=10,
center=", ".join(point[0]),
color=[
i * j for i, j in zip(
color_map(point[1] * (color_map.N - 1) /
(categories - 1)), [1, 1, 1, 0.3])
],
modelId=point[1],
modelName=point[2])
print "open %s" % reference
chimera.runCommand("open %s" % reference)
def mutate_nt(pam_idx, base):
"""Mutate a base pair at pam_idx to base
Args:
pam_idx: the index of the PAM nucleotide to be modified
base: what the nt at pam_idx will be changed to
"""
position_idx = {
0: "5.d",
1: "6.d",
2: "7.d",
3: "8.d"
} # Nucleotides we want to mutate are located at positions 5,6,7 in chain D (PAM,NGG) and 8,7,6 in chain C (target strand, NCC).
position_pairs = {
"5.d": "8.c",
"6.d": "7.c",
"7.d": "6.c",
"8.d": "5.c"
} # Create a dictionary mapping corresponding positions to each other.
base_pairs = {
'a': 't',
'c': 'g',
'g': 'c',
't': 'a'
} # Create dictionary mapping valid base pairs to each other.
pos = position_idx[pam_idx]
complement_base = base_pairs[base]
complement_pos = position_pairs[pos]
runCommand("swapna " + base + " : " + pos)
runCommand("swapna " + complement_base + " : " + complement_pos)
def openVolume(self):
try:
while True:
if self.vol_conn.poll():
msg = self.vol_conn.recv()
if msg == "open_volume":
data = self.vol_conn.recv() # objects are serialized by default
grid = Array_Grid_Data(data)
self.volume = volume_from_grid_data(grid)
elif msg == "voxel_size":
self.voxelSize = self.vol_conn.recv()
cmd = "volume #0 voxelSize %s" % self.voxelSize
runCommand(cmd)
elif msg == "command_list":
commandList = self.vol_conn.recv()
for command in commandList:
runCommand(command)
elif msg == "end": # if you don't break cicle volume is never shown
break
else:
sleep(0.01)
except EOFError:
print("Lost connection to client")
def abortRecording(self):
if not self.recording:
return
from chimera import runCommand
self.recording = False
runCommand("movie stop; movie reset")
self.status("Animation recording aborted")
def myRunCommand(*args): from Midas import MidasError try: runCommand(*args) except MidasError, v: from chimera import replyobj replyobj.status(str(v), color="red")
def set_center_of_rotation():
'Set center of rotation to center of selected atoms or use center of models mode if no atoms are selected'
from chimera import selection
if selection.currentEmpty():
chimera.runCommand('~cofr')
else:
chimera.runCommand('cofr sel')
def surface_selected_atoms():
'Show MSMS molecular surface enclosing just the selected atoms'
global surface_category_number
category_name = 'c%d' % surface_category_number
chimera.runCommand('surfcat %s sel' % category_name)
surface_category_number += 1
chimera.runCommand('surface %s' % category_name)
def openVolume(self):
try:
while True:
if self.vol_conn.poll():
msg = self.vol_conn.recv()
if msg == 'open_volume':
data = self.vol_conn.recv()#objects are serialized by default
grid = Array_Grid_Data(data)
self.volume = volume_from_grid_data(grid)
elif msg == 'voxel_size':
self.voxelSize = self.vol_conn.recv()
cmd = "volume #0 voxelSize %s"%self.voxelSize
runCommand(cmd)
elif msg == 'command_list':
commandList = self.vol_conn.recv()
for command in commandList:
runCommand(command)
elif msg == 'end':#if you don't break cicle volume is never shown
break
else:
sleep(0.01)
except EOFError:
print ('Lost connection to client')
def create_dm(pdbname, outputname):
# create density map
chan = chimera.openModels.open(pdbname)[0]
chimera.runCommand('molmap #0 %s modelId 1' % str(RESOULTION))
dm = chimera.specifier.evalSpec('#1').models()[0]
chan.destroy()
# rotate and save
translation = [0, 0, 0]
rot_phi = euler_xform([ANGLE_RES, 0, 0], translation)
rot_theta = euler_xform([0, ANGLE_RES, 0], translation)
rot_psi = euler_xform([0, 0, ANGLE_RES], translation)
for theta in range(0, 181, ANGLE_RES):
for phi in range(0, 360, ANGLE_RES):
for psi in range(0, 360, ANGLE_RES):
dm.openState.localXform(rot_psi)
angle_str = ''.join(
['_' + str(angle) for angle in [phi, theta, psi]])
np.save(outputname + angle_str, dm.matrix())
dm.openState.localXform(rot_psi)
dm.openState.localXform(rot_phi)
dm.openState.localXform(rot_phi)
dm.openState.localXform(rot_theta)
dm.close()
def main():
print sys.argv
if len(sys.argv) != 3: # if no input
print "ERROR: Wrong number of inputs"
print "syntax: chimera --nogui --script \"chimera_dockprep.py pdbinput output_prefix\""
print len(sys.argv)
return
#models = openModels.list(modelTypes=[chimera.Molecule])
input_pdb = sys.argv[1]
output_prefix = sys.argv[2]
print "pdb input = " + input_pdb
print "output prefix = " + output_prefix
#runCommand("open " + input_pdb)
#models = chimera.openModels.list(modelTypes=[chimera.Molecule])
#model = models
model = openModels.open(input_pdb)
#runCommand("del @H,H?,H??,H???") # remove all hydrogens
writeMol2(model, output_prefix + "before_dockprep.mol2")
prep(model)
runCommand("write 0 " + output_prefix + ".pdb")
writeMol2(model, output_prefix + ".mol2")
runCommand("del HC") # remove all non-polar hydrogens
runCommand("write 0 " + output_prefix + "_polarH.pdb")
runCommand("del @H,H?,H??,H???") # remove all hydrogens
runCommand("write 0 " + output_prefix + "_noH.pdb")
def runChimCommand(self, cmd):
if self.chimlog is not None:
f = open(self.chimlog, "a")
f.write(str(cmd)+"\n")
f.close()
#nogui_message(cmd.strip()+"\n")
chimera.runCommand(cmd)
def color_map(resolution):
import chimera
from chimera import runCommand
maxres = 3.93
minres = 6.7371428571428575
a = (resolution - maxres) / (minres - maxres)
r, g, b = 1 - a, 0.0, a
runCommand('color %0.2f,%0.2f,%0.2f,1.0 #1' % (r, g, b))
def Cancel(self):
from chimera import runCommand
from Midas import MidasError
try:
runCommand('movie reset')
except MidasError:
pass # Suppress error when user already reset movie by other means.
self.Close()
def Cancel(self):
from chimera import runCommand
from Midas import MidasError
try:
runCommand('movie reset')
except MidasError:
pass # Suppress error when user already reset movie by other means.
self.Close()
def run_command(self, *args, **kwargs):
"""
Get the contents of the CLI field and run them in Chimera.
"""
command = self.gui.clifield.get()
try:
chimera.runCommand(command)
except Midas.MidasError as e:
print e
self.gui.error(e.__str__())
def main():
print sys.argv
if len(sys.argv) != 3: # if no input
print "ERROR: Wrong number of inputs"
print "syntax: /nfs/software/chimera/current/bin/chimera --nogui --script 'chimera_rmsd.py temp.txt \"#0:107-115@N,CA,C,O #1:107-115@N,CA,C,O\" '"
print len(sys.argv)
return
#models = openModels.list(modelTypes=[chimera.Molecule])
input_list_file = sys.argv[1]
#output_prefix = sys.argv[2]
seltion_rmsd = sys.argv[2]
print "pdb inputs = " + input_list_file
#print "output prefix = " + output_prefix
print "seltion_rmsd = " + seltion_rmsd
fileh = open(input_list_file)
lines = fileh.readlines()
N = len(lines)
print "there are N systems:" + str(N)
fileh.close()
#seltion_align = "#0:1-115@N,CA,C,O #1:107-115@N,CA,C,O"
#seltion_rmsd = "#0:107-115@N,CA,C,O #1:107-115@N,CA,C,O"
#calulate alignment.
# this will already be aligned.
#templete = lines[0]
#runCommand("open "+ templete)
#for pdb_file in lines:
# runCommand("open "+ pdb_file)
# runCommand(ma
#seltion = "#0:111@N,CA,C,O #1:111@N,CA,C,O"
#seltion = "#0:108@N,CA,C,O #1:108@N,CA,C,O"
for i in range(0, N):
pdb_file1 = lines[i].strip('\n')
runCommand("open " + pdb_file1)
#for pdb_file2 in lines:
for j in range(i + 1, N):
pdb_file2 = lines[j].strip('\n')
print '\n########\n files: ' + pdb_file1 + " " + pdb_file2 + '\n########\n'
#sys.stdout = open(output_prefix+"_"+str(i)+"_"+str(i)+".txt", 'w')
runCommand("open " + pdb_file2)
runCommand("rmsd " + seltion_rmsd)
#print "rmsd_Text", rmsd_Text
runCommand("del #1")
#runCommand("write 0 "+output_prefix+"_polarH.pdb")
#sys.stdout.close()
runCommand("del #0")
def finish_recording(self):
self.recording = False
if self.play_handler:
self.stop_playing()
from chimera import runCommand
runCommand('movie stop')
self.save_movie_cb()
def revMainchainCmd(cmdName, args):
# We are going to implement ~mainchain as a synonym for "display",
# so we import runCommand which simplifies doing that.
from chimera import runCommand
from Midas import MidasError
if args:
# Raising MidasError will cause the error message
# to show up in the status line as red text
raise MidasError("~mainchain takes no arguments")
# runCommand takes any legal command-line command and executes it.
runCommand("display")
def generate_pam_variant_chimera(pam, input_pdb, output_dir):
"""Generate a new PDB file
Args:
pam: new PAM sequence to be listed in name
template_pdb_basename: original fine basename
output_dir: output directory
"""
template_pdb_basename = os.path.basename(input_pdb)
new_pdb_path = os.path.join(output_dir, template_pdb_basename[:-4] + "." + pam + ".pdb")
runCommand("write 0 " + new_pdb_path)
runCommand("close all")
def revMainchainCmd(cmdName, args):
# We are going to implement ~mainchain as a synonym for "display",
# so we import runCommand which simplifies doing that.
from chimera import runCommand
from Midas import MidasError
if args:
# Raising MidasError will cause the error message
# to show up in the status line as red text
raise MidasError("~mainchain takes no arguments")
# runCommand takes any legal command-line command and executes it.
runCommand("display")
def generate_pam_variant_chimera(pam, input_pdb, output_dir):
"""Generate a new PDB file
Args:
pam: new PAM sequence to be listed in name
template_pdb_basename: original fine basename
output_dir: output directory
"""
template_pdb_basename = os.path.basename(input_pdb)
new_pdb_path = os.path.join(
output_dir, template_pdb_basename[:-4] + "." + pam + ".pdb")
runCommand("write 0 " + new_pdb_path)
runCommand("close all")
def run(self):
if self._mi is None:
from chimera import UserError
raise UserError("Please finish adding hydrogens and "
"charges before trying to minimize")
import chimera
self._mi.setFixed(self.freeze)
self._mi.loadMMTKCoordinates()
chimera.runCommand("wait 1")
self._mi.minimize(nsteps=self.nsteps, stepsize=self.stepsize,
interval=self.interval,
action=self.updateCoords)
def html(*models):
if models:
for m in chimera.openModels.list():
m.display = False
chimera.selection.clearCurrent()
for model in models:
model.display = True
chimera.selection.addCurrent(model)
chimera.runCommand('focus sel')
chimera.viewer.windowSize = 800, 600
path = 'chimera_scene_export.html'
Midas.export(filename=path, format='WebGL')
return IFrame(path, *[x + 20 for x in chimera.viewer.windowSize])
def _endRecording(self, *args):
from Midas import MidasError
try:
from chimera import runCommand
runCommand("movie stop")
self.status("Compiling frames into animation", blankAfter=5)
runCommand("movie encode " + self.encodeArgs)
except:
self.status("Error stopping/encoding movie", color="red")
from chimera.replyobj import reportException
reportException("Error stopping/encoding movie")
from chimera.triggerSet import ONESHOT
return ONESHOT
def run(self):
if self._mi is None:
from chimera import UserError
raise UserError("Please finish adding hydrogens and "
"charges before trying to minimize")
import chimera
self._mi.setFixed(self.freeze)
self._mi.loadMMTKCoordinates()
chimera.runCommand("wait 1")
self._mi.minimize(nsteps=self.nsteps,
stepsize=self.stepsize,
interval=self.interval,
action=self.updateCoords)
def Apply(self):
path, format = self.getPathsAndTypes()[0]
from MovieRecorder import RecorderGUI
for fmt, f in RecorderGUI.command_formats.items():
if f[0] == format:
break
from CGLtk.Hybrid import float_variable_value
bit_rate = float_variable_value(self.bit_rate, self.default_bit_rate)
from chimera import runCommand
runCommand('movie encode mformat %s bitrate %f output "%s"'
% (fmt, bit_rate, path))
def clean_canvas(molecule):
chimera.runCommand('delete solvent')
for element in ('CA', 'NA'):
chimera.runCommand('sel @/element={}'.format(element))
if len(chimera.selection.currentAtoms()) > 1:
chimera.runCommand('del @/element={}'.format(element))
chimera.runCommand('delete @/element=NA')
def Apply(self):
path, format = self.getPathsAndTypes()[0]
from MovieRecorder import RecorderGUI
for fmt, f in RecorderGUI.command_formats.items():
if f[0] == format:
break
from CGLtk.Hybrid import float_variable_value
bit_rate = float_variable_value(self.bit_rate, self.default_bit_rate)
from chimera import runCommand
runCommand('movie encode mformat %s bitrate %f output "%s"' %
(fmt, bit_rate, path))
def runAlign():
# -----------------------------------------------------------------------------
### set files
#maindir = '/ami/data16/appion/09mar04b/models/emanmodel28'
default_settings.set('limit_voxel_count', False)
maindir = '/home/vossman/Documents/papers/initmodel/initmodels-figure'
map1_path = os.path.join(maindir, 'reconemdb.mrc')
map1 = open_volume_file(map1_path)[0]
map1.set_parameters(surface_levels = [1.0])
mrcfiles = glob.glob(os.path.join(maindir, '*.mrc'))
aligndir = os.path.join(maindir, 'align/')
if not os.path.isdir(aligndir):
os.mkdir(aligndir)
N = len(mrcfiles)
random.shuffle(mrcfiles)
for i,mrcfile in enumerate(mrcfiles):
if os.path.basename(mrcfile)[:5] == "align":
continue
new_path = os.path.join(aligndir, 'align'+os.path.basename(mrcfile))
if os.path.isfile(new_path):
print "----------", os.path.basename(mrcfile)
continue
print ("\n==============================\n",
os.path.basename(mrcfile),
"\n==============================\n")
map2 = open_volume_file(mrcfile)[0]
map2.set_parameters(surface_levels = [1.0])
new_path = os.path.join(aligndir, 'align'+os.path.basename(mrcfile))
fit_map_in_map(map1, map2, map1_threshold=1.0)
runCommand('vop #1 resample onGrid #0 modelId %d'%(i+N))
runCommand('volume #%d save %s'%(i+N, new_path))
map2.close()
runCommand('close #1')
runCommand('close #%d'%(i+N))
def chimera_smiles_btn_cb(self, *args, **kwargs):
molecules = self.bk_selected_molecules()
if not molecules:
return
from bkchem.oasa_bridge import mol_to_smiles
cmd = self.gui.ui_cmdline.getvalue()
for m in molecules:
smiles = mol_to_smiles(m)
cmol = chimera.openModels.open(smiles, type='SMILES')[0]
self.imported_molecules.append(cmol)
if cmd:
try:
chimera.runCommand(cmd.replace('#$', cmol.oslIdent()))
except chimera.UserError as e:
self.gui.status(str(e), color='red', blankAfter=3)
def _endRecording(self, *args):
from Midas import MidasError
try:
from chimera import runCommand
runCommand("movie stop")
self.status("Compiling frames into animation",
blankAfter=5)
runCommand("movie encode " + self.encodeArgs)
except:
self.status("Error stopping/encoding movie",
color="red")
from chimera.replyobj import reportException
reportException("Error stopping/encoding movie")
from chimera.triggerSet import ONESHOT
return ONESHOT
def mutate_nt(pam_idx, base):
"""Mutate a base pair at pam_idx to base
Args:
pam_idx: the index of the PAM nucleotide to be modified
base: what the nt at pam_idx will be changed to
"""
position_idx = { 0 : "5.d", 1 : "6.d", 2 : "7.d", 3 : "8.d"} # Nucleotides we want to mutate are located at positions 5,6,7 in chain D (PAM,NGG) and 8,7,6 in chain C (target strand, NCC).
position_pairs = { "5.d" : "8.c", "6.d" : "7.c", "7.d" : "6.c", "8.d" : "5.c"} # Create a dictionary mapping corresponding positions to each other.
base_pairs = {'a' : 't', 'c' : 'g', 'g' : 'c', 't' : 'a'} # Create dictionary mapping valid base pairs to each other.
pos = position_idx[pam_idx]
complement_base = base_pairs[base]
complement_pos = position_pairs[pos]
runCommand("swapna " + base + " : " + pos )
runCommand("swapna " + complement_base + " : " + complement_pos)
def main():
if len(sys.argv) != 3: # if no input
print "ERORR"
return
input_mol2 = sys.argv[1]
output_dms = sys.argv[2]
runCommand("open " + input_mol2)
# generate surface using 'surf' command
runCommand("surf")
# get the surf object
surf = openModels.list(modelTypes=[MSMSModel])[0]
# write DMS
writeDMS(surf, output_dms)
return
def _runCommand(self, cmd): import sys if not chimera.nogui: print "CMD", cmd.rstrip() sys.stdout.flush() try: from Midas import MidasError from chimera.oslParser import OSLSyntaxError from chimera import replyobj try: chimera.runCommand(cmd) except (MidasError, OSLSyntaxError), v: replyobj.error(str(v) + '\n') finally: if not chimera.nogui: print "\nEND" sys.stdout.flush()
def placeFragment(fragment, resName, model="scratch", position=None):
"""place a Fragment (see Fragment.py)
'resName' is the name of the new residue that will contain the
fragment. (It will be in the 'het' chain.)
'model' can either be a chimera.Molecule instance or a string.
If the latter, then a new model is created with the string as
its .name attribute.
'position' can either be a chimera.Point or None. If None, then
the fragment is positioned at the center of the view.
"""
if isinstance(model, basestring):
model = _newModel(model)
r = _newResidue(model, resName)
needFocus = False
if position is None:
if len(chimera.openModels.list()) == 1:
needFocus = True
xf = model.openState.xform
position = xf.inverse().apply(
Point(*chimera.viewer.camera.center))
# find fragment center
x = y = z = 0.0
for element, xyz in fragment.atoms:
x += xyz[0]
y += xyz[1]
z += xyz[2]
numAtoms = len(fragment.atoms)
fragCenter = Point(x / numAtoms, y / numAtoms, z / numAtoms)
correction = position - fragCenter
from chimera.molEdit import addAtom, genAtomName
atoms = []
for element, xyz in fragment.atoms:
atoms.append(addAtom(genAtomName(element, r), Element(element),
r, Point(*xyz) + correction))
for indices, depict in fragment.bonds:
r.molecule.newBond(atoms[indices[0]], atoms[indices[1]])
if needFocus:
chimera.runCommand("focus")
return r
def focus_binding_site(self, binding_site):
resname, chain, resid = binding_site.split(':')
try:
spec = ':{}.{}'.format(resid,
chain) if chain else ':{}'.format(resid)
chimera.runCommand('show {} zr < 5'.format(spec))
chimera.runCommand('focus {} zr < 5'.format(spec))
except MidasError:
spec = ':{}'.format(resname)
chimera.runCommand('show {} zr < 5'.format(spec))
chimera.runCommand('focus {} zr < 5'.format(spec))
def placeFragment(fragment, resName, model="scratch", position=None):
"""place a Fragment (see Fragment.py)
'resName' is the name of the new residue that will contain the
fragment. (It will be in the 'het' chain.)
'model' can either be a chimera.Molecule instance or a string.
If the latter, then a new model is created with the string as
its .name attribute.
'position' can either be a chimera.Point or None. If None, then
the fragment is positioned at the center of the view.
"""
if isinstance(model, basestring):
model = _newModel(model)
r = _newResidue(model, resName)
needFocus = False
if position is None:
if len(chimera.openModels.list()) == 1:
needFocus = True
xf = model.openState.xform
position = xf.inverse().apply(Point(*chimera.viewer.camera.center))
# find fragment center
x = y = z = 0.0
for element, xyz in fragment.atoms:
x += xyz[0]
y += xyz[1]
z += xyz[2]
numAtoms = len(fragment.atoms)
fragCenter = Point(x / numAtoms, y / numAtoms, z / numAtoms)
correction = position - fragCenter
from chimera.molEdit import addAtom, genAtomName
atoms = []
for element, xyz in fragment.atoms:
atoms.append(
addAtom(genAtomName(element, r), Element(element), r,
Point(*xyz) + correction))
for indices, depict in fragment.bonds:
r.molecule.newBond(atoms[indices[0]], atoms[indices[1]])
if needFocus:
chimera.runCommand("focus")
return r
def answer(self, msg):
"""execute a single command and return values"""
ChimeraServer.answer(msg)
if msg == "hk_icosahedron_lattice":
from IcosahedralCage import cages
h, k, radius, shellRadius, spheRadius, sym, sphere, color = self.vol_conn.recv()
###
# get vertexes of canonical triangle (20 per icosahedron)
# get triangles defined by h k for canonical triangle
corners, triangles, t_hex_edges = cages.hk_triangle(h, k)
# get vertex for icosahedron
# get vertex for each face
from Icosahedron import icosahedron_geometry
ivarray, itarray = icosahedron_geometry(sym)
tlist = []
# for a single face
# map triangles to a single face in the given orientation
for i0, i1, i2 in itarray:
face = ivarray[i0], ivarray[i1], ivarray[i2]
tmap = cages.triangle_map(corners, face)
tlist.extend(cages.map_triangles(tmap, triangles))
break #!!!!!!!!!!!!!!!!!!!!!!!!!
va, ta = cages.surface_geometry(tlist, tolerance=1e-5)
from numpy import multiply
multiply(va, shellRadius, va) # Scale to requested radius for point in va:
for point in va:
command = "shape sphere radius %s center %s,%s,%s color %s " % (
spheRadius,
point[0],
point[1],
point[2],
color,
)
runCommand(command)
self.vol_conn.send("axis")
self.vol_conn.send(va) # send serialized motion
def test():
import chimera
import AddH
m0, m1 = chimera.openModels.open("testdata/1dmo.pdb")
#m0, m1 = chimera.openModels.open("/mol/pdb/mt/pdb1mtx.ent")[:2]
minimize = True
if minimize:
AddH.simpleAddHydrogens([m0, m1])
m0.color = chimera.Color.lookup("red")
m1.color = chimera.Color.lookup("green")
chimera.runCommand("~disp ; ribbon; ribrepr sharp")
mm = MolecularMotion(m0, minimize=minimize)
mm.interpolate(m1)
mm.interpolate(m0)
from util import runMovie
runMovie(mm.trajectory())
def openVolume(self):
try:
while True:
if self.remote_conn.poll():
msg = self.remote_conn.recv()
#print msg
if msg == 'open_volume':
data = self.remote_conn.recv()
print data
grid = Array_Grid_Data(data)
self.volume = volume_from_grid_data(grid)
#runCommand("volume #0 step 1")
elif msg == 'voxelSize':
voxelSize = self.remote_conn.recv()
cmd = "volume #0 voxelSize %s"%voxelSize
runCommand(cmd)
runCommand("focus")
elif msg == 'draw_angular_distribution':
angulardist = self.remote_conn.recv()
for command in angulardist:
runCommand(command)
elif msg == 'end':
break
else:
sleep(0.01)
except EOFError:
print 'Lost connection to client'
def disp2D(self):
# print 1
self.fig1 = Figure(figsize=(4,4))
self.ax1 = self.fig1.add_subplot(111)
pt = geo.proj_sphere(self.ax.elev,self.ax.azim,self.p)
pt1 = geo.proj_sphere(self.ax.elev,self.ax.azim,self.p1)
#print self.ax.azim, self.ax.elev
# aa = pt[:,0]
#print aa.ndim
#print aa.shape
self.ax1.scatter(pt[:,0],pt[:,1],marker = 'o',c="goldenrod")
self.ax1.scatter(pt1[:,0],pt1[:,1],marker = '+',c="red")
self.canvas1 = FigureCanvasTkAgg(self.fig1, master=self.frame)
self.canvas1.get_tk_widget().grid(column=0,row=1)
#self.canvas2 = Tkinter.Canvas(self.frame,width=4,height=4)
#self.canvas2.configure(cursor="crosshair")
#self.canvas2.grid(column=0,row=1)
#self.canvas2.bind("<Button-1>", self.point)
cid1 = self.canvas1.mpl_connect('button_press_event', self.onclick1)
chimera.runCommand('turn x %f'%self.ax.azim)
print 'elev = %f, azim=%f,'%(self.ax.elev,self.ax.azim)
return
def record(self, fmin, fmax, fstep, f_changed_cb, roundtrip, save_movie_cb):
if self.recording:
return
self.f = self.fmin = fmin
self.fmax = fmax
self.fstep = fstep
self.f_changed_cb = f_changed_cb
self.save_movie_cb = save_movie_cb
self.recording = True
from math import ceil
steps = int(ceil((fmax - fmin) / fstep))
if roundtrip:
steps *= 2
from chimera import runCommand
runCommand('movie record')
self.play(fmin, fmin, fmax, fstep, f_changed_cb, 1, steps)
def main(self):
# prepare figure, frame, canvas
self.fig = plt.figure(figsize=(4,4))
self.frame = Tkinter.Frame(self)
self.frame.grid(padx=10,pady=10)
self.canvas = FigureCanvasTkAgg(self.fig, master=self.frame)
self.canvas.get_tk_widget().grid(column=0,row=0)
# define 3D interactive plot
self.ax = Axes3D(self.fig)
# display 3D model on chimera's main window
opened = chimera.openModels.open('class2_run10k_ct24_it031_class001.mrc')
tt=chimera.runCommand('volume #0 level 0.02 color pink')
# button widget to show the chosen angle
self.btn = Tkinter.Button(self,text=u'Chosen angle',command=self.disp2D)
self.btn.grid(column=0,row=2,sticky='EW')
cid = self.fig.canvas.mpl_connect('button_press_event', self.onclick)
# button widget for computing chronos and topos
self.btn = Tkinter.Button(self,text=u'Calculate Topos and Chronos now',command=self.disp2D)
self.btn.grid(column=0,row=3,sticky='EW')
cid = self.fig.canvas.mpl_connect('button_press_event', self.onclick)
# generate some fake data points
ss = 100
tt = 50
phi = np.ones((ss,1))
theta = np.ones((ss,1))
for i in range(phi.shape[0]):
phi[i] = random.uniform(0,2*np.pi)
theta[i] = random.uniform(0,np.pi)
phi1 = np.array([[0],[np.pi/2],[np.pi/20]])
theta1 = np.array([[0],[np.pi/2],[np.pi/20]])
phi1 = npm.repmat(phi1,tt,1)
theta1 = npm.repmat(theta1,tt,1)
self.p = geo.euler_to_vect(theta, phi)
self.p1 = geo.euler_to_vect(theta1, phi1)
self.points=[]
# display data points on the unit sphere
self.ax.view_init(elev=0, azim=90)
t = self.ax.scatter(self.p[:,0], self.p[:,1], self.p[:,2], marker='o', s=10, c="goldenrod", alpha=0.6)
t = self.ax.scatter(self.p1[:,0],self.p1[:,1],self.p1[:,2], marker='+', s=10, c="red", alpha=0.6)
# display data points that are in the front view
self.disp2D()
#
self.canvas2 = Tkinter.Canvas(self.frame,bg="white", width=4,height=4)
self.canvas2.configure(cursor="crosshair")
self.canvas2.grid(column=0,row=1)
self.canvas2.bind('<Button-1>', self.point)
def answer(self, msg):
# print msg
if msg == "open_volume":
data = self.vol_conn.recv() # objects are serialized by default
# print data
grid = Array_Grid_Data(data)
self.volume = volume_from_grid_data(grid)
self.centerVolume()
elif msg == "voxel_size":
self.voxelSize = self.vol_conn.recv()
cmd = "volume #0 voxelSize %s" % self.voxelSize
# print cmd
runCommand(cmd)
runCommand("focus")
# end debug
elif msg == "command_list":
commandList = self.vol_conn.recv()
for command in commandList:
runCommand(command)
def makeAllMeshes(proID, jobID, peptideLen=40, pocketDist=5.0):
global curResID
global curProID
global meshDir
global pocketMap
global resCount
global curJobID
#Insure input is a 4 character protein ID
proID = proID[0:4]
#Create a new directory for the protein
meshDir = proID + 'Mesh'
curProID = proID
curJobID = jobID
# os.mkdir(meshDir)
# os.system("chmod 777 " + meshDir)
try:
#Fetch protein from the PDB
runCommand('open '+ proID)
#Initial prep for pocket search
runCommand('delete solvent')
runCommand('delete :HOH')
#Open protein model
model = openModels.list(modelTypes=[Molecule])[0]
RES_LIST = model.residues
resCount = len(RES_LIST)
#Pocket finding procedure
chains = []
counts = []
index = 0
print 'Counting Chain Lengths................'
for res in RES_LIST:
curChain = str(res.id.chainId)
if len(chains) == 0:
chains.append(curChain)
counts.append(1)
if curChain != chains[index]:
index = index + 1
chains.append(curChain)
counts.append(1)
else:
counts[index] = counts[index] + 1
print 'Finding Peptide Ligand Pockets................'
for i, chain in enumerate(chains):
if counts[i] < peptideLen: #Less than X amino acids = peptide
runCommand('~select')
runCommand('select ligand & :.' + chain) #Check if actually ligand
runCommand('select selected zr<' + str(pocketDist)) #Select pocket
runCommand('~select :/isHet zr<' + str(pocketDist)) #De-select ligand
runCommand('~select ligand')
residues = selection.currentResidues() #Store pocket in memory
for res in residues:
if res in pocketMap:
pocketMap[res].append('|' + chain)
else:
pocketMap[res] = [chain]
print 'Finding non-Peptide Ligand Pockets................'
for res in RES_LIST:
if res.isHet: #Check if "heterogenous residue" which includes ligands
curResID = str(res.id)
runCommand('~select')
runCommand('select :' + curResID + ' & ligand') #Check if actually ligand
runCommand('select selected zr<' + str(pocketDist)) #Select pocket
runCommand('~select :' + curResID)
residues = selection.currentResidues() #Store pocket in memory
for pocketRes in residues:
if pocketRes in pocketMap:
pocketMap[pocketRes].append('|' + res.type + '-' + curResID)
else:
pocketMap[pocketRes] = [res.type + '-' + curResID]
print 'Dock Prep................'
prep(openModels.list(modelTypes=[Molecule]))
runCommand('delete ligand')
print '\nRunning Delphi................'
runCommand('~select')
runCommand('write format pdb 0 '+ proID + curJobID + '.pdb') #Write delphi-ready protein with hydrogens
#Create delphi parameter file
f = open('./param_' + curJobID, 'w')
f.write('in(pdb,file="'+ proID + curJobID + '.pdb")\n') #Input/Output files
f.write('in(siz,file="amber.siz")\n')
f.write('in(crg,file="amber.crg")\n')
f.write('out(phi,file="'+ proID + curJobID + '.phi")\n')
f.write('indi=2\n') #Interior dielectric constant
f.write('exdi=80.0\n') #Exterior dielectric constant (water)
f.write('prbrad=1.4\n')
f.write('salt=0.15\n') #Salt concentration and radius
f.write('ionrad=2.0\n')
# f.write('nonit=20\n') #Non-linear iterations
f.close()
os.system("./DELPHI_2004_LINUX_v2/delphi_static param_" + curJobID) #Run delphi
# print '\nExporting Mesh................'
runCommand('select #0')
runCommand('surface')
#runCommand('export format X3D ./' + proID + '.x3d') # Prints raw X3D file.
print '\nOpening Delphi Data................'
runCommand('open '+ proID + curJobID + '.phi')
runCommand('scolor #0 volume #1 cmap -1,red:0,white:1,blue;')
print '\nRemoving Temp Files................'
os.remove("./" + proID + curJobID + '.pdb')
os.remove("./" + proID + curJobID + '.phi')
os.remove('./param_' + curJobID)
print '\nDONE: ' + proID
except:
f = open("./" + 'ErrorLog' + curJobID + '.txt', 'w')
f.write(proID + ' error: ' + str(sys.exc_info()[0]) + str(sys.exc_info()[1]) + '\n')
f.close()
raise
import optparse
parser = optparse.OptionParser()
parser.add_option('--pqr_in', default=None, help='Input PQR file')
parser.add_option('--mol2_out', default=None, help='Output mol2 file')
(args, options) = parser.parse_args()
import os
if not os.path.exists(args.pqr_in):
raise Exception(args.pqr_in+' does not exist')
print 'Converting '+args.pqr_in+' to '+args.mol2_out
import chimera
chimera.openModels.open(args.pqr_in)
# Molecular surface
chimera.runCommand("addh")
chimera.runCommand("addcharge")
chimera.runCommand("write format mol2 0 "+args.mol2_out)
def updateCoords(self, mi):
import chimera
assert(self._mi is mi)
self._mi.saveMMTKCoordinates()
chimera.runCommand("wait 1")
# Issue this command inside Chimera
# 2dlabels create timer text "0 ns" color white ypos .9 xpos .9 size 50
# Issue this per-frame script
from chimera import runCommand
runCommand("2dlabels change timer text '%.1f ns'" % (mdInfo['frame']*0.02))
from chimera import runCommand
from chimera import openModels, Molecule
from os import chdir, listdir
import chimera
from WriteMol2 import writeMol2
import sys
file = open("com.txt")
for line in file:
if line.find("centroid has center") != -1:
#print "OPENED:%s" % line
word = line.split()
#print word
x = float(word[3])
y = float(word[4])
z = float(word[5]) + 16
center = Point(x, y, z)
runCommand("open " + sys.argv[1])
model0 = openModels.list(id=0, modelTypes=[Molecule])[0]
c = BuildStructure.placeHelium('com', model=model0, position=center)
runCommand("select He")
runCommand("namesel helium")
runCommand("select helium za>10")
runCommand("del sel")
runCommand("del helium")
writeMol2(chimera.openModels.list(modelTypes=[chimera.Molecule]), sys.argv[1][:-4] + ".mol2")
runCommand("close all")
# run with
## chimera --nogui olfr1392_1u19_noH.pdb writedms.py
## chimera --nogui pdb:3D7F_withoutLigand writedms.py
# chimera --nogui Q9I8C1_27_noH.pdb writedms.py
# where this py file is named writedms.py
# it would run chimera without gui on the file 3D7F_withoutLigand.pdb
# and it would output to a file called 3D7F_without_ligand.dms
from chimera import runCommand, openModels, MSMSModel
# generate surface using 'surf' command
runCommand("surf")
# get the surf object
surf = openModels.list(modelTypes=[MSMSModel])[0]
# write DMS
from WriteDMS import writeDMS
#writeDMS(surf, "3D7F_rec_noH.dms")
#writeDMS(surf, "olfr1392_1u19_noH.dms")
#writeDMS(surf, "Q9I8C1_27_aligned_noH.dms")
writeDMS(surf, "rec.dms")
import optparse
parser = optparse.OptionParser()
parser.add_option('--pdb_in', default=None, help='Input PDB file')
parser.add_option('--dms_out', default=None, help='Output dms file')
(args, options) = parser.parse_args()
import os
if not os.path.exists(args.pdb_in):
raise Exception(args.pdb_in+' does not exist')
print 'Processing '+args.pdb_in
import chimera
chimera.openModels.open(args.pdb_in)
# Molecular surface
from chimera import runCommand, openModels, MSMSModel
chimera.runCommand("surf") # generate surface using 'surf' command
surf = openModels.list(modelTypes=[MSMSModel])[0] # get the surf object
from WriteDMS import writeDMS
writeDMS(surf, args.dms_out) # write DMS
