def testExtend(self):
def check(v):
stored.v = None
cmd.do('foo', echo=0)
self.assertEqual(stored.v, v)
cmd.extend('foo', lambda: setattr(stored, 'v', 123))
check(123)
@cmd.extend
def foo():
stored.v = 456
check(456)
def __init__(self):
"""
This is the part that is automatically invoked on PyMOL startup.
"""
self.menuBar.addmenuitem("Plugin", "command", "Voronoia", label="Voronoia", command=lambda: start_voronoia(self))
if AUTOMATICALLY_OPEN_PYMOL_PLUGIN:
start_voronoia(self)
cmd.extend("packing", show_packing)
cmd.extend("packing_zscore", show_zscore)
cmd.extend("show_cavities", show_cavities)
cmd.extend("show_cav_neighbors", show_cav_neighbors)
def init(save=0, fetch=0, pymolapi=0):
'''
DESCRIPTION
Imports all psico submodules and puts "psico" into the pymol namespace
for GUI menus. Also enables "help psico" in the PyMOL command line.
ARGUMENTS
save = bool: Overload "save" command with psico.exporting.save (writes
secondary structure and crystal records to PDB header)
fetch = bool: Overload "fetch" command with psico.importing.fetch (can
fetch from local mirror, knows SCOP and CATH identifiers)
pymolapi = 0/1/2: Add all psico functions to PyMOL API (pymol.cmd)
'''
import pymol
from pymol import cmd
# init all submodules
psico = __import__(__name__, fromlist=__all__)
# pymol namespace
if not hasattr(pymol, 'psico'):
pymol.psico = psico
# pymol help
if 'psico' not in cmd.help_only:
cmd.help_only['psico'] = [psico]
cmd.help_sc.append('psico')
if save:
cmd.extend('save', psico.exporting.save)
if fetch:
cmd.extend('fetch', psico.importing.fetch)
if pymolapi:
init_cmd(pymolapi == 2)
def __init__(self):
print "initializing ProVAT viewer..."
provatpath = ''
if "PROVATPATH" not in os.environ.keys() :
provatpath = tkFileDialog.askdirectory(title = 'Provide path to ProVAT distribution', parent=self.root)
if not provatpath :
print "Cannot initialize ProVAT :-("
return
else : provatpath = os.environ["PROVATPATH"]
sys.path.append(provatpath)
print 'SYS.PATH', sys.path
from vorutil import Vorutil
cmd.extend('remvs',remvs)
cmd.extend('newvs',newvs)
cmd.extend('setAlpha',setAlpha)
cmd.extend('showvs',showvs)
cmd.extend('makesurf', makesurf)
print "initialized ProVAT successfully, enjoy !!"
self.menuBar.addmenuitem('Plugin', 'command', 'ProVAT', label='ProVAT', command = lambda s=self : initProvatWin(s))
provatData.provatframe = None
#!/usr/bin/env python
from pymol import cmd
def getrange(sel):
minid = min(cmd.identify(sel, 0))
maxid = max(cmd.identify(sel, 0))
print(str(minid) + '-' + str(maxid))
cmd.extend("getrange", getrange)
cmd.enable(cmpx)
cmd.select(selName1, 'none')
for (model,resi,diff) in stored.r:
key=resi+"-"+model
if abs(diff)>=float(cutoff):
if key in seen: continue
else: seen.append(key)
rVal.append( (model,resi,diff) )
# expand the selection here; I chose to iterate over stored.r instead of
# creating one large selection b/c if there are too many residues PyMOL
# might crash on a very large selection. This is pretty much guaranteed
# not to kill PyMOL; but, it might take a little longer to run.
cmd.select( selName1, selName1 + " or (%s and i. %s)" % (model,resi))
# this is how you transfer a selection to another object.
cmd.select(selName, cmpx + " in " + selName1)
# clean up after ourselves
cmd.delete(selName1)
cmd.delete(chA)
cmd.delete(chB)
cmd.delete(tempC)
# show the selection
cmd.enable(selName)
# reset users settings
cmd.set("dot_solvent", oldDS)
return rVal
cmd.extend("interfaceResidues", interfaceResidues)
fetch 1rx1, async=0
as cartoon
show surface
mset 1x80
movie.roll
movie_fade transparency, 1, 0., 40, 1.
movie_fade transparency, 41, 1., 80, 0.
SEE ALSO
mdo, mappend, set
"""
startFrame, endFrame, startVal = int(startFrame), int(endFrame), float(startVal)
endVal = abs(1.0 - startVal) if endVal is None else float(endVal)
if startFrame == endFrame:
raise CmdException("start == end")
if startFrame > endFrame:
startFrame, endFrame = endFrame, startFrame
startVal, endVal = endVal, startVal
for frame in range(startFrame, endFrame + 1):
frac = float(frame - startFrame) / (endFrame - startFrame)
value = (1.0 - frac) * startVal + frac * endVal
cmd.mappend(frame, "/cmd.set(%s, %f, %s)" % (repr(setting), value, repr(selection)))
cmd.extend("movie_fade", movie_fade)
cmd.auto_arg[0]["movie_fade"] = cmd.auto_arg[0]["set"]
# hacky: register working directory with test cases
dirname = os.path.abspath(os.path.dirname(filename))
PyMOLTestCase.moddirs[mod.__name__] = dirname
suite.addTest(unittest.defaultTestLoader
.loadTestsFromModule(mod))
testresult = unittest.TextTestRunner(stream=out,
resultclass=PyMOLTestResult,
verbosity=int(verbosity)).run(suite)
while deferred_unlink:
os.unlink(deferred_unlink.pop())
return len(testresult.errors) + len(testresult.failures)
def cli():
'''
Test suite client application.
'''
if not cliargs.filenames:
# silently do nothing
return
nfail = run_testfiles(**vars(cliargs))
cmd.quit(nfail)
cmd.extend('run_testfiles', run_testfiles)
cmd.set_object_ttt(self.name, m, homogenous=1)
def axes(name='axes'):
'''
DESCRIPTION
Puts coordinate axes to the lower left corner of the viewport.
'''
from pymol import cgo
auto_zoom = cmd.get('auto_zoom')
cmd.set('auto_zoom', 0)
w = 0.06 # cylinder width
l = 0.75 # cylinder length
h = 0.25 # cone hight
d = w * 1.618 # cone base diameter
obj = [cgo.CYLINDER, 0.0, 0.0, 0.0, l, 0.0, 0.0, w, 1.0, 0.0, 0.0, 1.0, 0.0, 0.0,
cgo.CYLINDER, 0.0, 0.0, 0.0, 0.0, l, 0.0, w, 0.0, 1.0, 0.0, 0.0, 1.0, 0.0,
cgo.CYLINDER, 0.0, 0.0, 0.0, 0.0, 0.0, l, w, 0.0, 0.0, 1.0, 0.0, 0.0, 1.0,
cgo.CONE, l, 0.0, 0.0, h+l, 0.0, 0.0, d, 0.0, 1.0, 0.0, 0.0, 1.0, 0.0, 0.0, 1.0, 1.0,
cgo.CONE, 0.0, l, 0.0, 0.0, h+l, 0.0, d, 0.0, 0.0, 1.0, 0.0, 0.0, 1.0, 0.0, 1.0, 1.0,
cgo.CONE, 0.0, 0.0, l, 0.0, 0.0, h+l, d, 0.0, 0.0, 0.0, 1.0, 0.0, 0.0, 1.0, 1.0, 1.0]
PutCenterCallback(name, 1).load()
cmd.load_cgo(obj, name)
cmd.set('auto_zoom',auto_zoom)
cmd.extend('axes', axes)
return (s1, s2)
def ccp4_contact( contactsfile, selName1 = "source", selName2 = "target" ):
# read and parse contacts file into two lists of contact atoms and contact pair list
s1, s2 = parseCONTACTContacts(open(contactsfile))
# create a selection for the first contact list
# create the PYMOL selection macros for the residues
resNames = [chain+"/"+residue+"/" for (type, residue, chain, atom) in s1]
# put them in a set to remove duplicates and then join with 'or'
resSel = " or ".join(frozenset(resNames))
# finally select them under the new name
cmd.select(selName1 + "_res", resSel)
atomNames = [chain+"/"+residue+"/"+atom for (type, residue, chain, atom) in s1]
atomSel = " or ".join(frozenset(atomNames))
cmd.select(selName1 + "_atom", atomSel)
# create a selection for the second contact list
resNames = [chain+"/"+residue+"/" for (type, residue, chain, atom) in s2]
resSel = " or ".join(frozenset(resNames))
cmd.select(selName2 + "_res", resSel)
atomNames = [chain+"/"+residue+"/"+atom for (type, residue, chain, atom) in s2]
atomSel = " or ".join(frozenset(atomNames))
cmd.select(selName2 + "_atom", atomSel)
cmd.extend("ccp4_contact", ccp4_contact)
# create the axes object, draw axes with cylinders coloured red, green,
#blue for X, Y and Z
com = (0.0, 0.0, 0.0)
if center_obj:
com = center_of_mass.get_com(center_obj)
u_vec = com/np.linalg.norm(com)
print 'Origin ', com
print 'Unit vector ', u_vec
obj = [
CYLINDER, com[0] - length, com[1], com[2], com[0] + length, com[1], com[2], radius, 1, 0, 0, 1, 0, 0,
CYLINDER, com[0], com[1] - length, com[2], com[0], com[1] + length, com[2], radius, 0, 1, 0, 0, 1, 0,
CYLINDER, com[0], com[1], com[2] - length, com[0], com[1], com[2] + length, radius,0, 0, 1, 0, 0, 1,
]
# add labels to axes object (requires pymol version 0.8 or greater, I
# believe
cyl_text(obj,plain,[com[0] - length, com[1], com[2]],'X',0.20,axes=[[3,0,0],[0,3,0],[0,0,3]])
cyl_text(obj,plain,[com[0], com[1] - length, com[2]],'Y',0.20,axes=[[3,0,0],[0,3,0],[0,0,3]])
cyl_text(obj,plain,[com[0], com[1], com[2] - length],'Z',0.20,axes=[[3,0,0],[0,3,0],[0,0,3]])
# then we load it into PyMOL
if center_obj:
cmd.load_cgo(obj, center_obj + '_axes')
else:
cmd.load_cgo(obj, 'axes')
cmd.extend('axes', plot_axis)
height = unittouu(height, dpi)
cmd.png(filename, width, height, dpi, ray)
def save_pdb_without_ter(filename, selection, *args, **kwargs):
'''
DESCRIPTION
Save PDB file without TER records. External applications like TMalign and
DynDom stop reading PDB files at TER records, which might be undesired in
case of missing loops.
'''
v = cmd.get_setting_boolean('pdb_use_ter_records')
if v: cmd.set('pdb_use_ter_records', 0)
cmd.save(filename, selection, *args, **kwargs)
if v: cmd.set('pdb_use_ter_records')
## pymol command stuff
cmd.extend('save_traj', save_traj)
cmd.extend('save_pdb', save_pdb)
cmd.extend('paper_png', paper_png)
cmd.auto_arg[1].update([
('save_traj', cmd.auto_arg[1]['save']),
('save_pdb', cmd.auto_arg[1]['save']),
])
# vi:expandtab:smarttab
cmd.disable(name)
# disables all estograms and then enables the ones you've selected
def enable_selected():
selected = list(set([int(x.resi) for x in cmd.get_model("sele").atom]))
for name in cmd.get_names("objects"):
if (name.startswith("esto_res")):
cmd.disable(name)
for seqpos in selected:
name = "esto_res%i"%seqpos
cmd.enable(name)
cmd.delete("sele")
cmd.set_key( 'CTRL-C' , enable_selected )
# restore the camera
cmd.set_view(save_view)
cmd.extend( 'lddt', do_lddt )
cmd.extend( 'lddt_interface', do_lddt_interface )
cmd.extend( 'lddt_path', set_lddt_path )
from chempy import cpv
def COM(selection='all', center=0, quiet=1):
model = cmd.get_model(selection)
nAtom = len(model.atom)
COM = cpv.get_null()
for a in model.atom:
COM = cpv.add(COM, a.coord)
COM = cpv.scale(COM, 1. / nAtom)
if not int(quiet):
print ' COM: [%8.3f,%8.3f,%8.3f]' % tuple(COM)
if int(center):
cmd.alter_state(1,
selection,
"(x,y,z)=sub((x,y,z), COM)",
space={
'COM': COM,
'sub': cpv.sub
})
return COM
cmd.extend("COM", COM)
for k, (sigma, w) in enumerate(zip(mixture.sigma, mixture.w)):
print(' %s_%d: sigma = %6.3f, w = %.3f' % (prefix, k + 1, sigma, w))
print(' BIC: %.2f' % (mixture.BIC))
print(' Log Likelihood: %.2f' % (mixture.log_likelihood))
# all those have kwargs: mobile, target, mobile_state, target_state
align_methods = [
'align', 'super', 'cealign', 'tmalign', 'theseus', 'prosmart', 'xfit'
]
align_methods_sc = cmd.Shortcut(align_methods)
# pymol commands
cmd.extend('alignwithanymethod', alignwithanymethod)
cmd.extend('tmalign', tmalign)
cmd.extend('dyndom', dyndom)
cmd.extend('gdt_ts', gdt_ts)
cmd.extend('local_rms', local_rms)
if 'extra_fit' not in cmd.keyword:
cmd.extend('extra_fit', extra_fit)
cmd.extend('intra_theseus', intra_theseus)
cmd.extend('theseus', theseus)
cmd.extend('prosmart', prosmart)
cmd.extend('xfit', xfit)
cmd.extend('intra_xfit', intra_xfit)
cmd.extend('promix', promix)
cmd.extend('intra_promix', intra_promix)
# autocompletion
maxY,
minZ, #7
VERTEX,
minX,
minY,
maxZ, #2
VERTEX,
minX,
maxY,
maxZ, #4
VERTEX,
maxX,
minY,
maxZ, #6
VERTEX,
maxX,
maxY,
maxZ, #8
END
]
boxName = "box_" + str(randint(0, 10000))
while boxName in cmd.get_names():
boxName = "box_" + str(randint(0, 10000))
cmd.load_cgo(boundingBox, boxName)
return boxName
cmd.extend("drawBoundingBox", drawBoundingBox)
curFile = "%s/frame-%04d.png" % (tmpdir, frame)
print("Created frame %i/%i (%0.0f%%)" % (frame + 1, samples, 100 *
(frame + 1) / samples))
# Save the image to temporary directory
if ray:
cmd.ray(width, height)
cmd.png(curFile)
else:
cmd.png(curFile, quiet=1)
# Create the average/blured image
try:
avg = Image.blend(avg, Image.open(curFile), 1.0 / (frame + 1))
except:
avg = Image.open(curFile)
# Return the protein and the light to the original orientation
cmd.set('light', light)
cmd.set_view(view)
# Load the blured image
avg.save('%s/avg.png' % (tmpdir))
cmd.load('%s/avg.png' % (tmpdir))
# Delete the temporary files
rmtree(tmpdir)
cmd.extend('FocalBlur', FocalBlur)
obj.append(cgo.NORMAL)
obj.extend(normal)
# need to order vertices to generate correct triangles for plane
if cpv.dot_product(cpv.sub(pos[0], pos[1]), cpv.sub(pos[2],
pos[3])) < 0:
vorder = [0, 1, 2, 2, 3, 0]
else:
vorder = [0, 1, 2, 3, 2, 1]
# fill in the vertex data for the triangles;
for i in vorder:
obj.append(VERTEX)
obj.extend(pos[i])
# finish the CGO
obj.append(END)
# update the UI
cmd.load_cgo(obj, name, state, zoom=0)
cmd.set("cgo_transparency", transp, name)
cmd.extend("bbPlane", bbPlane)
# tab-completion of arguments
cmd.auto_arg[0]['bbPlane'] = cmd.auto_arg[1]['color']
cmd.auto_arg[1]['bbPlane'] = cmd.auto_arg[0]['color']
# vi:expandtab
for j in range(numcol):
print "%4d %10.8g %10.8g %10.8g %10.8g %10.8g" % \
(j, mean[j], stdev[j], median[j],maximum[j], minimum[j])
count = 0
if number != 0:
print "Loading %d lowest energy structures: " % number
for i in range(number):
load_obj(data[i][0], obj, float(data[i][1]),i+1,discrete)
count += 1
else:
if level != 0.0:
print "Loading structures with energy below specified level: ",level
limit = level
else:
print "Loading structures with energy below the median: ",median
limit = median
for i in range(len(data)):
if float(data[i][1]) < limit:
load_obj(data[i][0], obj, float(data[i][1]),i+1,discrete)
count += 1
print 'Loaded %d structures into %s' % (count, obj)
cmd.extend('load_best',load_best)
tmatched, smatched, tmp_names = matchmaker(target, source, match)
key = '(' + ','.join(identifiers.split()) + ',)'
tkeys, skeys = [], []
cmd.iterate(tmatched, 'tkeys.append(%s)' % (key), space=locals())
cmd.iterate(smatched, 'skeys.append(%s)' % (key), space=locals())
t2s = dict(zip(tkeys, skeys))
cmd.alter(target, '%s = t2s.get(%s, %s)' % (key, key, key), space=locals())
for name in tmp_names:
cmd.delete(name)
if 'split_chains' not in cmd.keyword:
cmd.extend('split_chains', split_chains)
cmd.extend('split_molecules', split_molecules)
cmd.extend('rmsf2b', rmsf2b)
cmd.extend('set_sequence', set_sequence)
if 'alphatoall' not in cmd.keyword:
cmd.extend('alphatoall', alphatoall)
if 'mse2met' not in cmd.keyword:
cmd.extend('mse2met', mse2met)
cmd.extend('polyala', polyala)
cmd.extend('stub2ala', stub2ala)
cmd.extend('remove_alt', remove_alt)
cmd.extend('dssp', dssp)
cmd.extend('stride', stride)
cmd.extend('dss_promotif', dss_promotif)
cmd.extend('sst', sst)
cmd.extend('set_phipsi', set_phipsi)
cmd.color(WAT_COLOR["IPE_UNOCC"], "resn hoh and chain x" + extra)
cmd.set("sphere_scale", "0.1", "resn hoh and chain x" + extra)
cmd.color(WAT_COLOR["CRY_UNOCC"], "resn hoh and chain a" + extra)
cmd.set("sphere_scale", "0.2", "resn hoh and chain a" + extra)
cmd.show("spheres", "resn hoh" + extra)
cmd.set("label_position", (0,-1.5,0))
if os.path.exists(fName):
counter = 0
for eachLine in open(fName):
fields = eachLine.split()
if fields[0][:3] != "HOH": continue
chainId = fields[0][3]
resSeq = int(fields[0][-4:])
selection = ("resn hoh and chain %c and resi %d" % (chainId, resSeq)) + extra
if int(fields[1]) != DUMMY_WATER:
cmd.set("sphere_scale", "0.3", selection)
if chainId == 'A':
cmd.color(WAT_COLOR["CRY_OCC"], selection)
cmd.label(selection, '"A" + resi')
elif chainId == 'X':
cmd.color(WAT_COLOR["IPE_OCC"], selection)
cmd.label(selection, '"X" + resi')
counter += 1
print "%d occupied waters colored" % counter
cmd.extend("occupiedWaters", occupiedWaters)
DESCRIPTION
MMalign wrapper
Reference: S. Mukherjee and Y. Zhang, Nucleic Acids Research 2009; 37: e83
http://zhanglab.ccmb.med.umich.edu/MM-align/
SEE ALSO
tmalign, tmscore
'''
return tmalign(mobile, target, args, exe, ter, transform, quiet=quiet)
# pymol commands
cmd.extend('alignwithanymethod', alignwithanymethod)
cmd.extend('tmalign', tmalign)
cmd.extend('tmscore', tmscore)
cmd.extend('mmalign', tmalign)
# autocompletion
cmd.auto_arg[0].update({
'tmalign': cmd.auto_arg[0]['align'],
'tmscore': cmd.auto_arg[0]['align'],
'mmalign': cmd.auto_arg[0]['align'],
})
cmd.auto_arg[1].update({
'tmalign': cmd.auto_arg[1]['align'],
'tmscore': cmd.auto_arg[1]['align'],
'mmalign': cmd.auto_arg[1]['align'],
})
cmd.save(ligand_filename, ligand, state)
cmd.save(protein_filename, protein, state)
args = [exe, '-l', ligand_filename, '-p', protein_filename, '-t', '',
'-o', filename, '-s', str(width), str(height)]
if not quiet:
print(' poseview: running...')
process = subprocess.Popen(args,
universal_newlines=True,
stderr=subprocess.STDOUT, stdout=subprocess.PIPE)
stdout, _ = process.communicate()
if not quiet:
print(stdout)
print(' poseview: done')
if filename.endswith('.png'):
cmd.load(filename)
elif not quiet:
print(' Warning: cannot load "%s" into PyMOL, unsupported file type' % (filename))
except OSError:
print(' Error: Cannot execute "%s", please provide full path to poseview executable' % (exe))
raise CmdException
finally:
shutil.rmtree(tempdir)
cmd.extend('poseview', poseview)
for target in targets:
try:
search_results = subseq_ga_search(target, data, submatrix,
gapcost, minscore, firstonly)
except Exception as e:
logging.error("{0}".format(e))
continue
if search_results is not None:
select(search_results, target, sele, method='global')
else:
logging.info("Nothing can be found for given target: {0}"
.format(target))
cmd.extend('subseq', subseq_re)
cmd.extend('subseq.local', subseq_local_alignment)
cmd.extend('subseq.global', subseq_global_alignment)
stored.id = 0
class CallCounter:
"""Decorator to determine number of calls for a method"""
def __init__(self, method):
self.method = method
self.counter = 0
def __call__(self, *args, **kwargs):
self.counter += 1
return self.method(*args, **kwargs)
if not prefix:
prefix = os.path.basename(filename).rsplit('.', 1)[0]
for maptype in maptypes.split():
F, P, prg = header.guessCols(maptype)
if None in (F, P):
print ' Warning: No %s map' % (maptype)
continue
name = prefix + '.' + maptype
if not multistate:
cmd.delete(name)
cmd.map_generate(name, filename, F, P, 'None', 0, 0, quiet)
if name not in cmd.get_names('objects'):
print ' Error: Loading %s map failed.' % (maptype)
print ' This PyMOL version might not be capable of loading MTZ files'
raise CmdException
# commands
cmd.extend('loadall', loadall)
cmd.extend('load_traj_crd', load_traj_crd)
cmd.extend('load_traj_dcd', load_traj_dcd)
cmd.extend('load_3d', load_3d)
cmd.extend('load_aln', load_aln)
cmd.extend('load_gro', load_gro)
cmd.extend('load_mtz', load_mtz)
# vi:expandtab:smarttab
if chain in b_dict:
b = b_dict[chain][resi][name]
else:
b = b_dict[''][resi][name]
return b
stored.b = b_lookup
#Print table
for i in range(len(diff2)):
print resi[0][i], name[0][i], diff2[i]
for i in range(len(diff2)):
sum_rmsf += diff2[i]
try:
b_dict.setdefault(chain[0][i], {}).setdefault(
resi[0][i],
{})[name[0][i]] = diff2[i]**2 * 8 / 3 * math.pi**2
except KeyError:
print chain[0][i], resi[0][i], name[0][i]
cmd.alter(selection, '%s=stored.b(chain,resi,name)' % ('b'))
mean_rmsf = sum_rmsf / len(diff2)
# sys.stdout = orig_stdout
# fout.close()
print "Mean RMSF for selection: %s = %g" % (selection, mean_rmsf)
cmd.extend("rmsf_states", rmsf_states)
#-------------------------------------------------------------------------------
def disp_list():
print(
'''
quickdisplay - list of functions.
Enter, e.g. "help disp_ss" for more specific info.
PURPOSE FUNCTION
secondary structure cartoon......disp_ss
ball and stick representation....disp_ball_stick
mesh display.....................disp_mesh
surface display..................disp_surf
Putty b-factor sausage...........disp_putty
'''
)
cmd.extend( "disp_list", disp_list )
#-------------------------------------------------------------------------------
#-------------------------------------------------------------------------------
#-------------------------------------------------------------------------------
# PERCENTILE LIMITS (used below)
#-------------------------------------------------------------------------------
def get_b_limits(input='[0,100]', selection='all'):
from pymol import cmd, stored
import math
try:
limits=str(input)
# Create stick residue objects
for i in range(len(MaxNegDist)):
name = str(i) + "_" + str(round(MaxNegDist[i][0], 1)) + "_" + shortaa(str(MaxNegDist[i][5])) + str(MaxNegDist[i][1]) + shortaa(str(MaxNegDist[i][6])) + str(MaxNegDist[i][2])
selection = str(molecule1) + " and resi " + str(MaxNegDist[i][1]) + "+" + str(MaxNegDist[i][2]) + " or " + str(molecule2) + " and resi " + str(MaxNegDist[i][2])
# print selection
cmd.create(name, selection)
if showsticks == 'yes' or showsticks == 'y':
cmd.show("sticks", name)
for i in range(len(MaxPosDist)):
name = str(i) + "_" + str(round(MaxPosDist[i][0], 1)) + "_" + shortaa(str(MaxPosDist[i][5])) + str(MaxPosDist[i][1]) + shortaa(str(MaxPosDist[i][6])) + str(MaxPosDist[i][2])
selection = str(molecule1) + " and resi " + str(MaxPosDist[i][1]) + "+" + str(MaxPosDist[i][2]) + " or " + str(molecule2) + " and resi " + str(MaxPosDist[i][2])
# print selection
cmd.create(name, selection)
if showsticks == 'yes' or showsticks == 'y':
cmd.show("sticks", name)
cmd.extend("dispmap", dispmap)
def create_nXn_matrix(n):
return [[0.0 for x in range(n)] for x in range(n)]
def distance(array1, array2, i, j):
i = int(i)
j = int(j)
dist = sqrt((array1[i][0] - array2[j][0]) ** 2 + (array1[i][1] - array2[j][1]) ** 2 + (array1[i][2] - array2[j][2]) ** 2)
return dist
def Coord(Input):
print(cmd.get_atom_coords(Input))
'MET':'M',
'PHE':'F',
'PRO':'P',
'SER':'S',
'THR':'T',
'TRP':'W',
'TYR':'Y',
'VAL':'V'
}
return trans[three]
# ------------------------------------------------------------
# ************************************************************
# Expose to the PyMOL shell
cmd.extend('setup', setup)
cmd.extend('frag', frag)
cmd.extend('getRots', getRots)
cmd.extend('localSculpt', localSculpt)
cmd.extend('seq', seq)
# ------------------------------------------------------------
######################
# Modified avf.py
#####################
def writeCatSeq(variant):
# Convenience list of variants, replacing the '+'.
varlist = variant.split('+')
# Initialization of the bash script
if expression in discrete_expr:
val_range = int(maximum - minimum + 1)
else:
val_range = maximum - minimum
cmd.color(colors[0], selection)
steps = 60 / parts
steps_total = steps * parts
val_start = minimum
for p in range(parts):
for i in range(steps):
ii = float(i)/steps
col_list = [colvec[p+1][j] * ii + colvec[p][j] * (1.0 - ii) for j in range(3)]
col_name = '0x%02x%02x%02x' % (col_list[0] * 255, col_list[1] * 255, col_list[2] * 255)
val_end = val_range * (i + 1 + p * steps) / steps_total + minimum
if expression in discrete_expr:
cmd.color(col_name, '(%s) and %s %d-%d' % (selection, expression, val_start, val_end))
else:
cmd.color(col_name, '(%s) and %s > %f' % (selection, expression, val_start))
val_start = val_end
cmd.extend('spectrumany', spectrumany)
# tab-completion of arguments
cmd.auto_arg[0]['spectrumany'] = [ expression_sc , 'expression' , ', ' ]
cmd.auto_arg[1]['spectrumany'] = [ cmd.auto_arg[0]['color'][0], 'color', ' ' ]
cmd.auto_arg[2]['spectrumany'] = cmd.auto_arg[2]['spectrum']
# vi:expandtab:smarttab
if v.startswith('['):
return cmd.safe_list_eval(v)
return cmd.get_atom_coords(v)
xyz1 = get_coord(atom1)
xyz2 = get_coord(atom2)
normal = cpv.normalize(cpv.sub(xyz1, xyz2))
if hlength < 0:
hlength = radius * 3.0
if hradius < 0:
hradius = hlength * 0.6
if gap:
diff = cpv.scale(normal, gap)
xyz1 = cpv.sub(xyz1, diff)
xyz2 = cpv.add(xyz2, diff)
xyz3 = cpv.add(cpv.scale(normal, hlength), xyz2)
obj = [cgo.CYLINDER] + xyz1 + xyz3 + [radius] + color1 + color2 + \
[cgo.CONE] + xyz3 + xyz2 + [hradius, 0.0] + color2 + color2 + \
[1.0, 0.0]
if not name:
name = cmd.get_unused_name('arrow')
cmd.load_cgo(obj, name)
cmd.extend('cgo_arrow', cgo_arrow)
for i in it:
(start, stop) = i.span()
# we found some residues, which chains are they from?
i_chains = chains[start:stop]
# are all residues from one chain?
if len(set(i_chains)) != 1:
# now they are not, this match is not really a match, skip it
continue
chain = i_chains[0]
cmd.select(rSelName, rSelName + " or (__h and i. " + str(IDs[start]) + "-" + str(IDs[stop - 1]) + " and c. " + chain + " )")
if int(firstOnly):
break
cmd.delete("__h")
return rSelName
cmd.extend("findseq", findseq)
def checkParams(needle, haystack, selName, het, firstOnly):
"""
This is just a helper function for checking the user input
"""
# check Needle
if len(needle) == 0 or type(needle) != types.StringType:
print "Error: Please provide a string 'needle' to search for."
print "Error: For help type 'help motifFinder'."
return False
# check Haystack
if len(haystack) == 0 or type(haystack) != types.StringType:
print "Error: Please provide valid PyMOL object or selection name"
val_range = int(last - first + 1)
if val_range < 2:
print ' Error: no spectrum possible, need more than 1 state'
raise CmdException
for i in range(val_range):
p = float(i) / (val_range - 1) * (len(colvec) - 1)
p0, p1 = int(floor(p)), int(ceil(p))
ii = (p - p0)
col_list = [
colvec[p1][j] * ii + colvec[p0][j] * (1.0 - ii) for j in range(3)
]
col_name = '0x%02x%02x%02x' % (col_list[0] * 255, col_list[1] * 255,
col_list[2] * 255)
for s in settings:
cmd.set(s, col_name, selection, state=i + first)
cmd.extend('spectrum_states', spectrum_states)
# tab-completion of arguments
cmd.auto_arg[0]['spectrum_states'] = cmd.auto_arg[0]['disable']
cmd.auto_arg[1]['spectrum_states'] = [
cmd.auto_arg[0]['show'][0], 'representation', ' '
]
cmd.auto_arg[2]['spectrum_states'] = [
cmd.auto_arg[0]['color'][0], 'color', ' '
]
# vi:expandtab:smarttab
cmd.turn('z', 180)
cx = -view[12]; cy = -view[13]; cz = -view[14]
cameraZ = - view[11] - 150;
fov = float(cmd.get("field_of_view"))
fogStart = float(cmd.get("fog_start"))
slabNear = view[15] + view[11]
slabFar = view[16] + view[11]
ret += "\nview:%.3f,%.3f,%.3f,%.3f,%.3f,%.3f,%.3f,%.3f" % \
(cx, cy, cz, cameraZ, slabNear, slabFar, fogStart, fov)
for i in range(9):
ret += ",%.3f" % view[i]
bgcolor = cmd.get_setting_tuple('bg_rgb')[1]
ret += "\nbgcolor:%02x%02x%02x" % (int(255 * float(bgcolor[0])), \
int(255 * float(bgcolor[1])), int(255 * float(bgcolor[2])))
if 'PYMOL_GIT_MOD' in os.environ:
template = open(os.path.join(os.environ['PYMOL_GIT_MOD'],'pymol2glmol','imported.html')).read().\
replace("###INCLUDE_PDB_FILE_HERE###", cmd.get_pdbstr(name)).\
replace('###INCLUDE_REPRESENTATION_HERE###', ret)
else:
template = open('imported.html').read().\
replace("###INCLUDE_PDB_FILE_HERE###", cmd.get_pdbstr(name)).\
replace('###INCLUDE_REPRESENTATION_HERE###', ret)
f = open(name + '.html', 'w')
f.write(template)
f.close()
cmd.extend('pymol2glmol', dump_rep)
cmd.auto_arg[0]['pymol2glmol'] = [cmd.object_sc, 'object', '']
API only. Context manager to restore the current scene on exit.
'''
def __init__(self, **kwargs):
self.kwargs = kwargs
def __enter__(self):
import random
self.name = 'tmp_%d' % (random.randint(0, 1e8))
cmd.scene(self.name, 'store', **self.kwargs)
def __exit__(self, type, value, traceback):
cmd.scene(self.name, 'recall')
cmd.scene(self.name, 'delete')
# commands
cmd.alias('z', 'zoom visible')
cmd.alias('x', 'nice')
cmd.extend('nice', nice)
cmd.extend('cbm', cbm)
cmd.extend('cbs', cbs)
cmd.extend('spectrumany', spectrumany)
cmd.extend('spectrum_states', spectrum_states)
# tab-completion of arguments
cmd.auto_arg[0]['spectrumany'] = [ expression_sc , 'expression' , ', ' ]
cmd.auto_arg[1]['spectrumany'] = [ cmd.auto_arg[0]['color'][0], 'color', ' ' ]
cmd.auto_arg[2]['spectrumany'] = cmd.auto_arg[2]['spectrum']
cmd.auto_arg[0]['spectrum_states'] = cmd.auto_arg[0]['disable']
cmd.auto_arg[1]['spectrum_states'] = [ cmd.auto_arg[0]['show'][0], 'representation', ' ' ]
cmd.auto_arg[2]['spectrum_states'] = cmd.auto_arg[1]['spectrumany']
# vi:expandtab:smarttab
selection1Dictionary = createSelectionDictionary(selection1)
selection2Dictionary = createSelectionDictionary(selection2)
for key in selection1Dictionary:
if key in selection2Dictionary:
if selection1Dictionary[key] != selection2Dictionary[key]:
chainsAndResidues += conjunction + ' ( chain ' + key[
0] + ' and resi ' + key[1] + ' )'
conjunction = ' or'
if chainsAndResidues != '':
cmd.do('select %s, (%s or %s) and (%s)' %
(selection3, selection1, selection2, chainsAndResidues))
cmd.extend("diffSelections", diffSelections)
#####################################################
# MSL Stuff
import PythonMSL
def localSamplingCCD(
system="all",
fragSel="sele and name CA",
bbqTable="/export/home/brettth/projectsS/code/tree/mslib/trunk/tables/PiscesBBQTable.txt",
angle=10,
numResults=25):
cmd.read_pdbstr(
PythonMSL.localSamplingCCD(cmd.get_pdbstr(system),
cmd.get_pdbstr(fragSel), numResults, angle,
# check for obsolete development version of pymolplugins
if 'pymolplugins' in sys.modules:
from .legacysupport import tkMessageBox
tkMessageBox.showwarning('WARNING',
'"pymolplugins" now integrated into PyMOL as "pymol.plugins"! '
'Please remove the old pymolplugins module and delete ~/.pymolrc_plugins.py')
if os.path.exists(PYMOLPLUGINSRC):
from pymol import parsing
parsing.run_file(PYMOLPLUGINSRC, {'__script__': PYMOLPLUGINSRC}, {})
autoload = (pmgapp != -2)
for parent in [startup]:
modules = findPlugins(parent.__path__)
for name, filename in modules.items():
mod_name = parent.__name__ + '.' + name
info = PluginInfo(name, filename, mod_name)
if autoload and info.autoload:
info.load(pmgapp)
# pymol commands
cmd.extend('plugin_load', plugin_load)
cmd.extend('plugin_pref_save', pref_save)
# autocompletion
cmd.auto_arg[0]['plugin_load'] = [ lambda: cmd.Shortcut(plugins), 'plugin', '' ]
# vi:expandtab:smarttab:sw=4
cara = "CA"
if stored.resdict[b] == "GLY":
carb = "CA"
#cmd.distance(f"{a}_{b}_{model}",f"(/{model}//{chain}/{a}/{cara})",(f"(/{model}//{chain}/{b}/{carb})"))
cmd.distance('{0}_{1}_{2}'.format(a, b, model),
'/{0}//{1}/{2}/{3}'.format(model, chain, a, cara),
'/{0}//{1}/{2}/{3}'.format(model, chain, b, carb))
cmd.set('dash_color', 'cyan')
cmd.set('dash_radius', '0.1')
cmd.set('dash_gap', '0.05')
print("===finished===")
cmd.extend('contactmap', contactmap)
# tab-completion of arguments
cmd.auto_arg[0].update({
'contactmap': cmd.auto_arg[0]['zoom'],
})
def contactmap_yang(selection='',
chain='',
align='hmm2.map',
pcut=0.999,
offset=0):
'''
DESCRIPTION
b_dict = dict()
for col in cmd.get_raw_alignment(aln):
assert len(col) == 2
b = cpv.distance(idx2coords[col[0]], idx2coords[col[1]])
for idx in col:
b_dict[idx] = b
#pdb.set_trace()
cmd.alter(seleboth, 'b = b_dict.get((model, index), -1)', space=locals())
if doPretty:
cmd.orient(seleboth)
cmd.show_as('cartoon', 'byobj ' + seleboth)
cmd.color('gray', seleboth)
cmd.spectrum('b', 'blue_red', seleboth + ' and b > -0.5')
if not quiet:
print " ColorByRMSD: Minimum Distance: %.2f" % (min(b_dict.values()))
print " ColorByRMSD: Maximum Distance: %.2f" % (max(b_dict.values()))
print " ColorByRMSD: Average Distance: %.2f" % (sum(b_dict.values()) / len(b_dict))
cmd.delete(aln)
cmd.delete(seleboth)
cmd.extend('colorbyrmsd', colorbyrmsd)
# tab-completion of arguments
cmd.auto_arg[0]['colorbyrmsd'] = cmd.auto_arg[0]['align']
cmd.auto_arg[1]['colorbyrmsd'] = cmd.auto_arg[1]['align']
# vi: ts=4:sw=4:smarttab:expandtab
+ " \t\t=>\t HELIX: " + str(round(aaDict[aa][0] / sum(aaDict[aa]), 3)) + " %"
+ " \t BETA: " + str(round(aaDict[aa][1] / sum(aaDict[aa]), 3)) + " %"
+ " \t LOOP: " + str(round(aaDict[aa][2] / sum(aaDict[aa]), 3)) + " %"
)
def countStructuresForAA(aa="ALA", elemName="all"):
"""
Detects for a single amino acid how
:param aa: 3 letter code amino acid
:param elemName: all
:return: list of counts in [helices, betasheet, loops, total amount]
"""
structurList = [0, 0, 0] # [H,S,L]
objList = cmd.get_names("objects")
obj = objList[0] # elements (right in the protein browser in pymol)
models = cmd.get_model(obj + " and resn " + aa + " and name CA")
for i in models.atom:
if i.ss == "H":
structurList[0] += 1 # counting the Helix
elif i.ss == "S":
structurList[1] += 1
else:
structurList[2] += 1
return structurList
#make function usable in PyMol
cmd.extend("countStructuresForAA", countStructuresForAA)
cmd.extend("countStructuresForAllAA", countStructuuresForAllAA)
for (a,_) in ref:
f.write("<li><a href='#%s'>%s</a>" % (a, a))
f.write("</ul>")
for (a, func) in ref:
doc = func.__doc__.strip().replace("<", "<")
f.write("<hr size=1><h2 id='%s'>%s</h2>" % (a, a))
f.write("<pre>%s</pre>" % (doc))
f.write("<p class='api'>api: %s.%s</p>" % (func.__module__, func.__name__))
f.write("</body></html>")
f.close()
def write_txt_ref(filename, prefix='psico'):
'''
DESCRIPTION
Write psico command and its DESCRIPTION to file as plain text.
SEE ALSO
cmd.write_html_ref
'''
write_html_ref(filename, prefix, 'txt_short')
cmd.extend('grepset', grepset)
cmd.extend('apropos', apropos)
cmd.extend('api_info', api_info)
cmd.auto_arg[0]['api_info'] = [ cmd.kwhash, 'command', '' ]
# vi:expandtab:smarttab
pmgapp == -1: Autoloading but no legacyinit
else: Autoloading and legacyinit
'''
if os.path.exists(PYMOLPLUGINSRC):
from pymol import parsing
try:
parsing.run_file(PYMOLPLUGINSRC, {'__script__': PYMOLPLUGINSRC},
{})
except SyntaxError as e:
colorprinting.warning(str(e))
autoload = (pmgapp != -2)
for parent in [startup]:
modules = findPlugins(parent.__path__)
for name, filename in modules.items():
mod_name = parent.__name__ + '.' + name
info = PluginInfo(name, filename, mod_name)
if autoload and info.autoload:
info.load(pmgapp)
# pymol commands
cmd.extend('plugin_load', plugin_load)
cmd.extend('plugin_pref_save', pref_save)
# autocompletion
cmd.auto_arg[0]['plugin_load'] = [lambda: cmd.Shortcut(plugins), 'plugin', '']
# vi:expandtab:smarttab:sw=4
except CmdException:
print('FAILED: %s - %s' % (sele1, sele2))
print(restraints["ID"])
return 0
else:
if single:
label = "NOE"
else:
label = "NOE_" + restraints["ID"]
try:
cmd.distance(label, sele1, sele2, quiet=quiet,
width=line_width, gap=0, label=0)
_color_restraint(label, line_color)
except CmdException:
print('FAILED: %s - %s' % (sele1, sele2))
print(restraints["ID"])
return 0
return 1
def _color_restraint(object_name, color="yellow"):
cmd.set("dash_color", color, object_name)
cmd.extend("plot_noe", plot_noe)
def __init_plugin__(app):
cmd.extend('showAlignment', showAlignment)
refRes = node.get('residue')
refPos = node.get('aaPosition')
intPos = int(refPos) + 1
except:
print('no ref')
continue
# snp alleles
for node in rs.xpath(addr % ('missense'), namespaces=ns):
pos = node.get('aaPosition')
assert pos == refPos
features.add(('VARIANT', intPos, intPos, '%s -> %s (in dbSNP:rs%s)' % \
(refRes, node.get('residue'), rsId)))
# make SwissProt like record
record = Record()
record.entry_name = seq.id
record.sequence = str(seq.seq)
record.features = sorted(features)
snp_common(record, selection, label, name, quiet)
cmd.extend('snp_uniprot', snp_uniprot)
cmd.extend('snp_ncbi', snp_ncbi)
# tab-completion of arguments
cmd.auto_arg[1].update({
'snp_uniprot' : cmd.auto_arg[0]['zoom'],
'snp_ncbi' : cmd.auto_arg[0]['zoom'],
})
# vi:expandtab
cmd.save(pname, complex_name + ' and not resn ' + ResId)
cmd.delete(complex_name)
# Now deal with changing to complexes.
for complex in pdbfiles:
# copy the file over
# cmd.do('set retain_order,1')
new_complex_path = os.path.join(Complex_path, complex)
new_ligand_path = os.path.join(Ligand_path, complex)
# copy file
copyfile(new_complex_path, new_ligand_path)
# name, file extension
complex_name, file_ext = complex.split('.')
cmd.load(complex)
cmd.save(complex_name + '.pdb', complex_name + ' and resn ' + ResId)
cmd.delete(complex_name)
# Change dir back
os.chdir(maindir)
return pdbfiles
cmd.extend('LigandRMSProcess', LigandRMSProcess)
cmd.extend('ComplexRMSProcess', ComplexRMSProcess)
cmd.extend('ComplexFP', ComplexFP)
cmd.extend('LigandFP', LigandFP)
License: BSD-2-Clause
'''
from pymol import cmd
def show_bumps(selection='(all)', name='bump_check', quiet=1):
'''
DESCRIPTION
Visualize VDW clashes
ARGUMENTS
selection = string: atom selection {default: all}
name = string: name of CGO object to create {default: bump_check}
'''
cmd.delete(name)
cmd.create(name, selection, zoom=0)
cmd.set('sculpt_vdw_vis_mode', 1, name)
cmd.set('sculpt_field_mask', 0x020) # cSculptVDW
for state in range(1, 1 + cmd.count_states('%' + name)):
cmd.sculpt_activate(name, state)
strain = cmd.sculpt_iterate(name, state, cycles=0)
if not int(quiet):
print('VDW Strain in state %d: %f' % (state, strain))
cmd.show_as('cgo', name)
cmd.extend('show_bumps', show_bumps)
align_mine target=name1, files=cluster*.xyz
"""
file_list = glob.glob(files)
file_list.sort()
extension = re.compile( '(^.*[\/]|\.(pdb|ent|brk|xyz))' )
object_list = []
rmsd = {}
rmsd_list = []
for i in range(len(file_list)):
obj_name1 = extension.sub('',file_list[i])
object_list.append(extension.sub('',file_list[i]))
cmd.load(file_list[i],obj_name1)
objectname = 'align_%s_on_%s' % (object_list[i],target)
rms = cmd.align('%s '%(object_list[i]),'%s '%(target),object=objectname)
rmsd[object_list[i]] = (rms[0],rms[1])
rmsd_list.append((object_list[i],rms[0],rms[1]))
cmd.delete(obj_name1)
print ("Aligning against: %s"%(target))
for object_name in object_list:
print ("%s: %6.3f using %d atoms" % (object_name,rmsd[object_name][0],rmsd[object_name][1]))
for r in rmsd_list:
print ("%s: %6.3f using %d atoms" % r)
cmd.extend('align_mine',align_mine)
html.append('</font><font color="' + color + '">')
stored.color = color
html.append(aa)
for obj in cmd.get_object_list('(' + selection + ')'):
for chain in cmd.get_chains('model %s and (%s)' % (obj, selection)):
sele = 'model %s and chain "%s" and (%s)' % (obj, chain, selection)
html.append('\n<br>>%s_%s<font>' % (obj, chain))
stored.resv = None if gapped else 0
stored.color = None
cmd.iterate(sele, 'callback(resv, resn, color)', space=locals())
html.append('</font>')
handle = open(filename, 'w')
print('<html><body style="font-family:monospace">', file=handle)
print(''.join(html), file=handle)
print('</body></html>', file=handle)
handle.close()
cmd.extend('fasta', fasta)
cmd.extend('pir', pir)
cmd.extend('save_colored_fasta', save_colored_fasta)
cmd.auto_arg[0].update({
'fasta' : cmd.auto_arg[0]['zoom'],
'pir' : cmd.auto_arg[0]['zoom'],
})
cmd.auto_arg[1].update([
('save_colored_fasta', cmd.auto_arg[0]['zoom']),
])
# vi: ts=4:sw=4:smarttab:expandtab
coord1 = (m1.atom[0].coord, )
coord2 = (m2.atom[0].coord, )
cyl_obj = []
for x, y in zip(coord1, coord2):
cyl_obj.extend([CYLINDER] + x + y + [radius] + tup_color + tup_color2)
if not object_name:
if "link" not in cmd.get_names("objects"):
object_name = "link"
else:
count = 0
for n in cmd.get_names("objects"):
if n[0:4] == "link":
count += 1
object_name = "link" + str(count)
else:
count = 0
for n in cmd.get_names("objects"):
if n[0:len(object_name)] == object_name:
# print(object_name, n[0:len(object_name)])
count += 1
object_name = object_name # + str(count)
cmd.load_cgo(cyl_obj, object_name)
cmd.extend("draw_links", draw_links)
cmd.bg_color('white')
class set_temporary(object):
'''
DESCRIPTION
API only. Supports the following pattern:
>>> with set_temporary(pdb_retain_ids=1):
... cmd.save('out.pdb')
'''
def __init__(self, *args, **kwargs):
self.sele = kwargs.pop('selection', '')
self.args = args + tuple(kwargs.items())
def __enter__(self):
self.saved = []
for k, v in self.args:
v_saved = cmd.get(k, self.sele)
if v != v_saved:
self.saved.append((k, v_saved))
cmd.set(k, v, self.sele)
return self
def __exit__(self, type, value, traceback):
for k, v in self.saved:
cmd.set(k, v, self.sele)
cmd.extend('save_settings', save_settings)
cmd.extend('paper_settings', paper_settings)
# vi:expandtab:smarttab
atoms[0].adjacent.append(atoms[1])
atoms[1].adjacent.append(atoms[0])
minmax = [start, start]
def traverse(atom, resi):
atom.resi = resi
atom.visited = True
for other in atom.adjacent:
if other.visited:
continue
if (atom.name, other.name) in [('C', 'N'), ("O3'", 'P')]:
minmax[1] = resi + 1
traverse(other, resi + 1)
elif (atom.name, other.name) in [('N', 'C'), ('P', "O3'")]:
minmax[0] = resi - 1
traverse(other, resi - 1)
elif (atom.name, other.name) not in [('SG', 'SG')]:
traverse(other, resi)
traverse(startatom, start)
cmd.alter(selection,
'resi = atom_it.next().resi',
space={'atom_it': iter(model.atom)})
if not quiet:
print ' Renumber: range (%d to %d)' % tuple(minmax)
cmd.extend('renumber', renumber)
# vi:expandtab:smarttab
cmd.alter(sel+" and element C", "vdw=3.40") # 2.00 + 1.4
cmd.alter(sel+" and element N", "vdw=4.15") # 1.75 + 1.4 + 1.0
cmd.alter(sel+" and element O", "vdw=3.95") # 1.55 + 1.4 + 1.0
cmd.alter(sel+" and element H", "vdw=2.40") # 1.00 + 1.4
cmd.alter(sel+" and element P", "vdw=3.55") # 2.15 + 1.4
cmd.alter(sel+" and element S", "vdw=3.30") # 1.90 + 1.4
cmd.set("sphere_scale", 1.0)
def show_SASA_radii(sel="all"):
cmd.alter(sel+" and element C", "vdw=3.40") # 2.00 + 1.4
cmd.alter(sel+" and element N", "vdw=3.15") # 1.75 + 1.4
cmd.alter(sel+" and element O", "vdw=2.95") # 1.55 + 1.4
cmd.alter(sel+" and element H", "vdw=2.40") # 1.00 + 1.4
cmd.alter(sel+" and element P", "vdw=3.55") # 2.15 + 1.4
cmd.alter(sel+" and element S", "vdw=3.30") # 1.90 + 1.4
cmd.set("sphere_scale", 1.0)
def show_Rosetta_radii(sel="all"):
cmd.alter(sel+" and element C", "vdw=2.00")
cmd.alter(sel+" and element N", "vdw=1.75")
cmd.alter(sel+" and element O", "vdw=1.55")
cmd.alter(sel+" and element H", "vdw=1.00")
cmd.alter(sel+" and element P", "vdw=2.15")
cmd.alter(sel+" and element S", "vdw=1.90")
cmd.set("sphere_scale", 1.0)
cmd.extend('show_SASA_radii_expanded_polars',show_SASA_radii_expanded_polars)
cmd.extend('show_SASA_radii',show_SASA_radii)
cmd.extend('show_Rosetta_radii',show_Rosetta_radii)
if (state != None):
x, y, z = get_com(selection, mass=mass, quiet=quiet)
if not quiet:
print "%f %f %f" % (x, y, z)
cmd.pseudoatom(object, pos=[x, y, z], **kwargs)
cmd.show("spheres", object)
else:
for i in range(cmd.count_states()):
x, y, z = get_com(selection, mass=mass, state=i + 1, quiet=quiet)
if not quiet:
print "State %d:%f %f %f" % (i + 1, x, y, z)
cmd.pseudoatom(object, pos=[x, y, z], state=i + 1, **kwargs)
cmd.show("spheres", 'last ' + object)
cmd.extend("com", com)
def get_com(selection, state=1, mass=None, quiet=1):
"""
DESCRIPTION
Calculates the center of mass
Author: Sean Law
Michigan State University
slaw (at) msu . edu
"""
quiet = int(quiet)
totmass = 0.0
atoms1 = read_buried_unsats_from_logfile( fname1 )
atoms2 = read_buried_unsats_from_logfile( fname2 )
set_ats1 = set( atoms1 )
set_ats2 = set( atoms2 )
ats_intersect = set_ats1.intersection( set_ats2 )
ats_1_absent_2 = set_ats1.difference( set_ats2 )
ats_2_absent_1 = set_ats2.difference( set_ats1 )
obj_common = []
obj_common.extend( white )
append_sphere_objs_from_atoms( ats_intersect, obj_common )
obj_diff1 = []
obj_diff1.extend( blue )
append_sphere_objs_from_atoms( ats_1_absent_2, obj_diff1 )
obj_diff2 = []
obj_diff2.extend( red )
append_sphere_objs_from_atoms( ats_2_absent_1, obj_diff2 )
cmd.load_cgo(obj_common,'both buns',1)
cmd.load_cgo(obj_diff1,'set1 - set2',1)
cmd.load_cgo(obj_diff2,'set2 - set1',1)
cmd.extend("buried_unsats_from_logfile", buried_unsats_from_logfile )
cmd.extend("contrast_unsats_logfile", contrast_unsats_logfile )
print("Unknown mode", mode)
def ccp4_ncont(contactsfile, selName1="source", selName2="target"):
# read and parse contacts file into two lists of contact atoms and contact pair list
s1, s2, pairs = parseNCONTContacts(open(contactsfile))
# create a selection for the first contact list
# create the PYMOL selection macros for the residues
resNames = [chain + "/" + residue + "/" for (type, chain, residue, atom) in s1]
# put them in a set to remove duplicates and then join with 'or'
resSel = " or ".join(frozenset(resNames))
# finally select them under the new name
cmd.select(selName1 + "_res", resSel)
atomNames = [chain + "/" + residue + "/" + atom for (type, chain, residue, atom) in s1]
atomSel = " or ".join(frozenset(atomNames))
cmd.select(selName1 + "_atom", atomSel)
# create a selection for the second contact list
resNames = [chain + "/" + residue + "/" for (type, chain, residue, atom) in s2]
resSel = " or ".join(frozenset(resNames))
cmd.select(selName2 + "_res", resSel)
atomNames = [chain + "/" + residue + "/" + atom for (type, chain, residue, atom) in s2]
atomSel = " or ".join(frozenset(atomNames))
cmd.select(selName2 + "_atom", atomSel)
cmd.extend("ccp4_ncont", ccp4_ncont)
try:
aa1 = to_one_letter_code[a1[0][0]]
aa2 = to_one_letter_code[a2[0][0]]
u_sum += matrix[i].get(aa1, aa2)
count += 1
except:
print('Failed for', a1[0], a2[0])
value = float(u_sum) / twoN
if not quiet:
print('PMF: %.4f (%d contacts, %d residues)' % (value, count, twoN))
return value
try:
from pymol import cmd
cmd.extend('aaindex2b', aaindex2b)
cmd.extend('pmf', pmf)
def pymol_auto_arg_update():
aaindexkey_sc = cmd.Shortcut(_aaindex.keys())
cmd.auto_arg[0].update({
'aaindex2b': [aaindexkey_sc, 'aaindexkey', ', '],
'pmf': [aaindexkey_sc, 'aaindexkey', ', '],
})
cmd.auto_arg[1].update({
'aaindex2b': [cmd.selection_sc, 'selection', ''],
})
cmd.auto_arg[2].update({
'pmf': [cmd.selection_sc, 'selection', ''],
})
cmd.auto_arg[3].update({
if len(high_sel) > 0:
cmd.show_as('dashes', HBO_name)
cmd.color('green', HBO_name)
high_sel.sort()
if not quiet:
hb.sort(lambda x,y:(cmp(x[0][1],y[0][1])))
print "--------------------------------------------------------------------"
print "------------------------------Results ------------------------------"
print "--------------------------------------------------------------------"
print " Donor | Aceptor |"
print " Object Chain Residue | Object Chain Residue | # wrappers wrapping"
for line in low_sel:
print line[1]
for line in mean_sel:
print line[1]
for line in high_sel:
print line[1]
print '\nProtein global statistics:'
print '\nz-score wrappers = %6.2f\nz-score hydrogen bonds = %6.2f\n' % (z_score_wrappers, z_score_hb)
elif not quiet and len(hb) != 0:
print '\n - no dehydrons were found - '
print '\nz-score hydrogen bonds = %6.2f\n' % (z_score_hb)
else:
print '\n - no hydrogen bonds were found - '
cmd.extend('wrappy', dehydron)
# vi:expandtab:smarttab
if v.startswith('['):
return cmd.safe_list_eval(v)
return cmd.get_atom_coords(v)
xyz1 = get_coord(atom1)
xyz2 = get_coord(atom2)
normal = cpv.normalize(cpv.sub(xyz1, xyz2))
if hlength < 0:
hlength = radius * 3.0
if hradius < 0:
hradius = hlength * 0.6
if gap:
diff = cpv.scale(normal, gap)
xyz1 = cpv.sub(xyz1, diff)
xyz2 = cpv.add(xyz2, diff)
xyz3 = cpv.add(cpv.scale(normal, hlength), xyz2)
obj = [cgo.CYLINDER] + xyz1 + xyz3 + [radius] + color1 + color2 + \
[cgo.CONE] + xyz3 + xyz2 + [hradius, 0.0] + color2 + color2 + \
[1.0, 0.0]
if not name:
name = cmd.get_unused_name('arrow')
cmd.load_cgo(obj, name)
cmd.extend('cgo_arrow', cgo_arrow)
r = cmd.get_raw_alignment(aln)
if names == ():
known_objs = []
map(known_objs.extend, map(lambda x: map(lambda y: y[0], x), r))
known_objs = set(known_objs)
# highest number of matches seen
M = max(map(len, r)) + 1
else:
known_objs = set(names)
M = len(known_objs) + 1
for obj in known_objs:
_self.alter(obj, "b=0.0")
for af in r:
c = float(1.0 + len(af)) / float(M)
for y in af:
_self.alter("%s and index %s" % (y[0], y[1]), "b=c", space={'c': c})
if as_putty != 0:
for obj in known_objs:
_self.show_as("cartoon", "%s" % obj)
_self.cartoon("putty", "%s" % obj)
_self.spectrum('b', color, obj)
_self.sort()
_self.rebuild()
return None
cmd.extend("color_by_conservation", color_by_conservation)