def setAutoDockElements(self, mol, typeAtoms=0, reassign=False):
if os.path.splitext(mol.parser.filename)[-1]=='.pdbqt' and reassign is False:
if self.verbose:
print 'setAutoDockElements unnecessary:\n', mol.name, ' already has AD4 atomtypes: not reassigned!'
return
#check that the types have already been set, first
if self.set_aromatic_carbons:
#this sets the autodock_element for the planar cyclic carbons to 'A'
aromatic_carbons = self.acm.setAromaticCarbons(mol)
d = {}
ah = AtomHybridization()
if not len(mol.allAtoms.bonds[0]):
mol.buildBondsByDistance()
ats_with_babel_type = filter(lambda x: hasattr(x, 'babel_type'), mol.allAtoms)
if typeAtoms or len(ats_with_babel_type)!=len(mol.allAtoms):
if self.verbose:
print "assigning babel_types"
ah = AtomHybridization()
ah.assignHybridization(mol.allAtoms)
for item in mol.allAtoms:
if not hasattr(item, 'autodock_element'):
#item.element = item.element.upper()
item.autodock_element = item.element
if item.element=='H':
if len(item.bonds):
n = item.bonds[0].neighborAtom(item)
if n.element not in ['C','A']:
item.autodock_element = 'HD'
else:
#note: if there are no bonds, assume HD
item.autodock_element = 'HD'
elif item.element=='N':
#this has already been done at beginning of for loop
#if item.babel_type in ['N3+','Ntr', 'Nox']:
# item.autodock_element = 'N'
if item.babel_type in ['N3','N2','N1']:
item.autodock_element = item.element + 'A'
elif item.babel_type in ['Nam', 'Npl', 'Ng+']:
if len(item.bonds)==2:
item.autodock_element = item.element + 'A'
elif item.element=='O':
item.autodock_element = item.element + 'A'
elif item.element=='S':
#possible sulphur babel_types->['S3+','S3','S2','Sac','Sox','S']
if item.babel_type not in ['Sox', 'Sac']:
item.autodock_element = item.element + 'A'
elif item.element=='C':
if item.parent.type+'_' + item.name in self.pep_aromList:
item.autodock_element = 'A'
if self.renameAtoms: #
if len(item.name)==1:
item.name = 'A'
else:
item.name = 'A' + item.name[1:]
elif hasattr(item, 'autodock_element'):
item.autodock_element = item.autodock_element
d[item.autodock_element] = 1
type_list = d.keys()
type_list.sort()
mol.types = type_list
def addCharges(self, atoms):
"""
compute gasteiger charges, add them to atoms, return list of new
charges
NB: assumes MolKit atoms have bonds
NB: calls type atoms if all the atoms haven't been babel typed.
if babel_types have been set by hand, they will be ok IF every
atom has a babel type
"""
#print 'in computeGasteiger'
#check that atoms have babel_types
w_babel_types = atoms.get(lambda x: hasattr(x, 'babel_type'))
if w_babel_types is None or len(w_babel_types)!=len(atoms):
babel = AtomHybridization()
#have to have bonds for this
babel.assignHybridization(atoms)
Gast = Gasteiger()
Gast.compute(atoms)
gastCharges = []
for c in atoms.gast_charge:
gastCharges.append(round(c, 4))
#NB THIS adds entry 'gasteiger' to atom._charges dict
atoms.addCharges('gasteiger', gastCharges)
atoms.chargeSet = 'gasteiger'
#clean-up
delattr(atoms, 'gast_charge')
return gastCharges
def getHBAtoms(mol):
"""
Function to identify donor and acceptor atoms for hydrogen bonds
d2, d3, a2, a3 <- getHBAtoms(mol)
The function will first build bonds then assign atom hybridization
and bond orders. Next it will use a HydrogenBondBuilder to identify and'
report donor and acceptor atoms in sets corresponding to Sp2 and Sp3
hybridization.
A .hbstatus is added to all atoms. The value can be:
NE: NEutral
D2: Sp2 donor
D3: Sp3 donor
A2: Sp2 acceptor
A3: Sp3 acceptor
B2: Sp2 acceptor and donor
B3: Sp3 acceptor and donor
"""
# add bonds
mol.buildBondsByDistance()
atoms = mol.allAtoms
# assign .babel_type
from PyBabel.atomTypes import AtomHybridization
atyper = AtomHybridization()
atyper.assignHybridization(atoms)
# assign bond order
from PyBabel.bo import BondOrder
bond_orderer = BondOrder()
bond_orderer.assignBondOrder(atoms, atoms.bonds[0])
# get donors
from MolKit.hydrogenBondBuilder import HydrogenBondBuilder
hbbuilder = HydrogenBondBuilder()
donorTypes = hbbuilder.paramDict['donorTypes']
donorsp2Ats, donorsp3Ats = hbbuilder.getHBDonors(atoms, donorTypes)
# get acceptors
acceptorTypes = hbbuilder.paramDict['acceptorTypes']
acceptorsp2Ats, acceptorsp3Ats = hbbuilder.getHBAcceptors(atoms, acceptorTypes)
# create hbstatus attribute
atoms.hbstatus = 'NE'
for a in donorsp2Ats:
a.hbstatus = 'D2'
for a in donorsp3Ats:
a.hbstatus = 'D3'
for a in acceptorsp2Ats:
a.hbstatus = 'A2'
for a in acceptorsp3Ats:
a.hbstatus = 'A3'
# handle atoms that are both donors and acceptor
for a in donorsp2Ats.inter(acceptorsp2Ats):
a.hbstatus = 'B2'
for a in donorsp3Ats.inter(acceptorsp3Ats):
a.hbstatus = 'B3'
return donorsp2Ats, donorsp3Ats, acceptorsp2Ats, acceptorsp3Ats
def check_babel_types(self, ats):
try:
ats.babel_type
ats._bndtyped
except AttributeError:
babel = AtomHybridization()
bond_orderer = BondOrder()
tops = ats.top.uniq()
for mol in tops:
babel.assignHybridization(mol.allAtoms)
bond_orderer.assignBondOrder(mol.allAtoms, mol.allAtoms.bonds[0])
mol.allAtoms._bndtyped = 1
def check_babel_types(self, ats):
num_ats = len(ats)
num_babel_type = len(ats.get(lambda x: hasattr(x, 'babel_type')))
num_bnd_type = len(ats.get(lambda x: hasattr(x, 'bnd_type')))
if (num_babel_type!=num_ats) or (num_bnd_type!=num_ats):
babel = AtomHybridization()
bond_orderer = BondOrder()
tops = ats.top.uniq()
for mol in tops:
babel.assignHybridization(mol.allAtoms)
bond_orderer.assignBondOrder(mol.allAtoms, mol.allAtoms.bonds[0])
mol.allAtoms._bndtyped = 1
def select(self, bnds, bondOrder=1):
ats = self.getAtoms(bnds)
mols = ats.top.uniq()
atype = AtomHybridization()
for m in mols:
if not m.chains[0].hasBonds:
m.buildBondsByDistance()
allAts = m.chains.residues.atoms
atype.assignHybridization(allAts)
rf = RingFinder()
rf.findRings2(allAts, allAts.bonds[0])
bo = BondOrder()
bo.assignBondOrder(allAts, allAts.bonds[0], rf)
return BondSet(bnds.get(lambda x, ord=bondOrder: x.bondOrder==ord))
def getLigandBondDict(self):
ats = self.allAtoms
babel = AtomHybridization()
babel.assignHybridization(self.allAtoms)
#typeBonds???
#typeAtoms(ats)
rf = RingFinder()
rf.findRings2(ats, ats.bonds[0])
ct = 1
bondDict = {}
for ring in rf.rings:
bondDict[ct] = ring['bonds']
for b in ring['bonds']:
b.cyclenum = ct
ct = ct + 1
self.cyclecount = rf.ringCount
self.bondDict = bondDict
def select(self, bnds):
ats = self.getAtoms(bnds)
rf = RingFinder()
#nb maxSize of ring is 20 by default
rf.findRings2(ats, bnds, maxSize=len(ats))
ats = self.getAtoms(rf.allRingBonds)
allAts = ats.top.uniq().allAtoms
atype = AtomHybridization()
atype.assignHybridization(allAts)
bo = BondOrder()
bo.assignBondOrder(allAts, allAts.bonds[0], rf)
arom = Aromatic(rf)
arom.find_aromatic_atoms(ats)
aromatic_bnds = ats.bonds[0].get(lambda x: x.bondOrder=='aromatic')
aromatic_ats = self.getAtoms(aromatic_bnds)
aromatic_ats.aromatic = 1
return aromatic_bnds
def computeGasteiger(self):
#to compute Gasteiger need to:
# create an AtomHybridization()
# call its assignHybridization method on self.allAtoms
# create a Gasteiger()
# call its compute method on self.allAtoms
# THEN move gast_charge into _charges with gasteiger key
# set allAtoms.chargeSet to 'gasteiger'
# THEN delattr gast_charge from allAtoms
allAts = self.allAtoms
ah = AtomHybridization()
ah.assignHybridization(allAts)
Gast = Gasteiger()
Gast.compute(allAts)
gastCharges = []
for c in allAts.gast_charge:
gastCharges.append(round(c, 3))
allAts.addCharges('gasteiger', gastCharges)
del allAts.gast_charge
allAts.chargeSet = 'gasteiger'
def computeGasteiger(self):
#to compute Gasteiger need to:
# create an AtomHybridization()
# call its assignHybridization method on self.allAtoms
# create a Gasteiger()
# call its compute method on self.allAtoms
# THEN move gast_charge into _charges with gasteiger key
# set allAtoms.chargeSet to 'gasteiger'
# THEN delattr gast_charge from allAtoms
allAts = self.allAtoms
ah = AtomHybridization()
ah.assignHybridization(allAts)
Gast = Gasteiger()
Gast.compute(allAts)
gastCharges = []
for c in allAts.gast_charge:
gastCharges.append(round(c, 3))
allAts.addCharges('gasteiger', gastCharges)
del allAts.gast_charge
allAts.chargeSet = 'gasteiger'
def addHydrogens(self, mol):
#check for bonds
if len(mol.allAtoms.bonds[0]) == 0:
mol.buildBondsByDistance()
bonds = mol.allAtoms.bonds[0]
#could have preset babel_types
#so check if allAtoms are already typed
try:
t = mol.allAtoms.babel_type
except:
#if all are not pretyped, type them
babel = AtomHybridization()
babel.assignHybridization(mol.allAtoms)
if self.method == 'withBondOrder':
mol.rings = RingFinder()
mol.rings.findRings2(mol.allAtoms, mol.allAtoms.bonds[0])
mol.rings.bondRings = {}
for ind in xrange(len(mol.rings.rings)):
r = mol.rings.rings[ind]
for b in r['bonds']:
if not mol.rings.bondRings.has_key(b):
mol.rings.bondRings[b] = [
ind,
]
else:
mol.rings.bondRings[b].append(ind)
bo = BondOrder()
bo.assignBondOrder(mol.allAtoms, bonds, mol.rings)
mol.allAtoms._bndtyped = 1
# do aromatic here
arom = Aromatic(mol.rings)
arom.find_aromatic_atoms(mol.allAtoms)
hat = AddHydrogens().addHydrogens(mol.allAtoms, method=self.method)
bondedAtomDict = {} # key is heavy atom
for a in hat:
if bondedAtomDict.has_key(a[1]):
bondedAtomDict[a[1]].append(a)
else:
bondedAtomDict[a[1]] = [a]
# now create Atom object for hydrogens
# and add the to the residues's atom list
molNewHs = AtomSet([]) # list of created H atoms for this molecule
heavyAtoms = AtomSet([]) # list of atoms that need new radii
for heavyAtom, HatmsDscr in bondedAtomDict.items():
#don't add hydrogens to carbons: polar Only!!!
if self.htype != 'all' and heavyAtom.element == 'C':
continue
res = heavyAtom.parent
# find where to insert H atom
childIndex = res.children.index(heavyAtom) + 1
# loop over H atoms description to be added
# start at the end to number correctly
l = len(HatmsDscr)
for i in range(l - 1, -1, -1):
a = HatmsDscr[i]
# build H atom's name
if len(heavyAtom.name) == 1:
name = 'H' + heavyAtom.name
else:
name = 'H' + heavyAtom.name[1:]
# if more than 1 H atom, add H atom index
# for instance HD11, HD12, Hd13 (index is 1,2,3)
if l > 1:
name = name + str(i + 1)
# create the H atom object
atom = Atom(name,
res,
top=heavyAtom.top,
chemicalElement='H',
childIndex=childIndex,
assignUniqIndex=0)
# set atoms attributes
atom._coords = [a[0]]
if hasattr(a[1], 'segID'): atom.segID = a[1].segID
atom.hetatm = 0
atom.alternate = []
#atom.element = 'H'
atom.occupancy = 1.0
atom.conformation = 0
atom.temperatureFactor = 0.0
atom.babel_atomic_number = a[2]
atom.babel_type = a[3]
atom.babel_organic = 1
atom.radius = 1.2
# create the Bond object bonding Hatom to heavyAtom
bond = Bond(a[1], atom, bondOrder=1)
# add the created atom the the list
molNewHs.append(atom)
# in case this new hydrogen atom ever ends up in pmv
# HAVE TO CREATE THESE ENTRIES
# create the color entries for all geoemtries
# available for the heavyAtom
for key, value in heavyAtom.colors.items():
atom.colors[key] = (0.0, 1.0, 1.0)
atom.opacities[key] = 1.0
mol.allAtoms = mol.chains.residues.atoms
if self.renumber:
mol.allAtoms.number = range(1, len(mol.allAtoms) + 1)
return len(molNewHs)
def add_oxt(self, catom):
if catom.element != 'C':
return
mol = catom.top
##check for bonds
#if len(mol.allAtoms.bonds[0])==0:
# mol.buildBondsByDistance()
#check whether residue already has OXT
res = catom.parent
if 'OXT' in res.atoms.name:
print('not adding OXT to ', res.full_name(), '\n',
'it already has an OXT atom')
return
#check whether catom has a hydrogen to delete
hatoms = catom.parent.atoms.get(lambda x: x.name == 'HC')
if len(hatoms):
hatom = hatoms[0]
#check for hbonds
if hasattr(hatom, 'hbonds'):
#remove hbonds
for b in hatom.hbonds:
atList = [b.donAt, b.accAt]
if b.hAt is not None:
atList.append(b.hAt)
for at in atList:
#hbonds might already be gone
if not hasattr(at, 'hbonds'):
continue
okhbnds = []
for hb in at.hbonds:
if hb != b:
okhbnds.append(hb)
if len(okhbnds):
at.hbonds = okhbnds
else:
delattr(at, 'hbonds')
#remove covalent bonds
for b in hatom.bonds:
at2 = b.atom1
if at2 == hatom: at2 = b.atom2
at2.bonds.remove(b)
hatom.parent.remove(hatom, cleanup=1)
#have to type atoms before call to add_sp2_hydrogen:
if not hasattr(catom, 'babel_type'):
print('catom has no babel_type: calling typeAtoms')
#self.warningMsg(msg)
#typeAtoms does whole molecule
babel = AtomHybridization()
babel.assignHybridization(mol.allAtoms)
#NB: bond_length 1.28 measured from OXT-C bond in 1crn
tup1 = self.addh.add_sp2_hydrogen(catom, 1.28)
res = catom.parent
# find where to insert H atom
childIndex = res.children.index(catom) + 1
name = 'OXT'
# create the OXT atom object
atom = Atom(name,
res,
top=mol,
childIndex=childIndex,
assignUniqIndex=0)
# set atoms attributes
atom._coords = [tup1[0][0]]
if hasattr(catom, 'segID'): atom.segID = catom.segID
atom.hetatm = 0
atom.alternate = []
atom.element = 'O'
atom.occupancy = 1.0
atom.conformation = 0
atom.temperatureFactor = 0.0
atom.babel_atomic_number = 8
atom.babel_type = 'O-'
atom.babel_organic = 1
# create the Bond object bonding Hatom to heavyAtom
bond = Bond(catom, atom, bondOrder=2)
# create the color entries for all geometries
# available for the other oxygen atom attached to 'C'
oatom = res.atoms.get(lambda x: x.name == 'O')[0]
if oatom is not None:
for key, value in list(oatom.colors.items()):
atom.colors[key] = value
#atom.opacities[key] = oatom.opacities[key]
# update the allAtoms set in the molecule
mol.allAtoms = mol.chains.residues.atoms
# update numbers of allAtoms
fst = mol.allAtoms[0].number
mol.allAtoms.number = list(range(fst, len(mol.allAtoms) + fst))
# update _uniqIndex of this residues atoms
res.assignUniqIndex()
#return AtomSet([atom])
return atom
def arrange_hydrogens(inputfile, outputfile, path=None):
if path and path not in sys.path:
sys.path.append(path)
from MolKit import Read
from PyBabel.atomTypes import AtomHybridization
from babel import ArrangeHydrogens
mol = Read(inputfile)
base, ext = os.path.splitext(inputfile)
# remove hydrogens from structure
inputfile_noH = base + '_noH' + ext
subprocess.check_output('babel -imol2 %s -omol2 %s -d &>/dev/null' %
(inputfile, inputfile_noH),
shell=True,
executable='/bin/bash')
molnoH = Read(inputfile_noH)
allAtoms = mol.allAtoms
allAtomsNoH = molnoH.allAtoms
babel = AtomHybridization()
babel.assignHybridization(allAtoms)
babel.assignHybridization(allAtomsNoH)
# get mol2 ids of all atoms and all hydrogens
ff = Reader(inputfile)
struct = ff.next()
hat_mol2_ids = []
at_mol2_ids = []
for line in struct['ATOM']:
atom_name = line[5]
#print line[2]
if atom_name[0] in ['H', 'h']:
hat_mol2_ids.append(line[0])
at_mol2_ids.append(line[0])
hat_mol2_ids = map(int, hat_mol2_ids)
at_mol2_ids = map(int, at_mol2_ids)
# find out the heavy atom each hydrogen is bound with
at_with_hat_mol2_ids = []
for id in hat_mol2_ids:
for line in struct['BOND']:
line_s = line.split()
origin_atom_id = int(line_s[1])
target_atom_id = int(line_s[2])
#print origin_atom_id
if id == origin_atom_id:
at_with_hat_mol2_ids.append(target_atom_id)
elif id == target_atom_id:
at_with_hat_mol2_ids.append(origin_atom_id)
if len(at_with_hat_mol2_ids) != len(hat_mol2_ids):
raise ValueError(
"Each hydrogen should have only one bound! Check you .mol2 file")
addh = ArrangeHydrogens()
# at_with_hat_idxs are the indices of atoms related to each hydrogen of hat
hat, at_with_hat_idxs = addh.addHydrogens(allAtoms, allAtomsNoH)
hat_coords = []
hat_done_mol2_ids = []
for idx, at_with_hat_idx in enumerate(at_with_hat_idxs):
at_with_hat_mol2_id = at_mol2_ids[at_with_hat_idx]
hat_mol2_ids_cur = [hat_mol2_ids[jdx] for jdx, id in enumerate(at_with_hat_mol2_ids) \
if id == at_with_hat_mol2_id]
kdx = 0
while hat_mol2_ids_cur[kdx] in hat_done_mol2_ids:
kdx += 1
hat_done_mol2_ids.append(hat_mol2_ids_cur[kdx])
hat_coords.append(hat[idx][0])
for line in struct['ATOM']:
id = int(line[0])
if id in hat_done_mol2_ids:
idx = hat_done_mol2_ids.index(id)
line[2:5] = ["%.4f" % coords for coords in hat_coords[idx]]
Writer().write(outputfile, struct)
os.remove(inputfile_noH)
if len(resPSet) > 1:
msg = resP.name + " specifies more than one residue:" + resP.full_name(
)
raise msg
resP = resPSet[0]
if verbose:
print "receptor residue is %s which has %d atoms" % (resP.full_name(),
len(resP.atoms))
#initialize the ligand
lM = Read(ligand_filename)[0]
if verbose: print 'read ', ligand_filename
lM.buildBondsByDistance() # try to assign bond order;set to 1 if exception
#lM.allAtoms.bonds[0].bondOrder = 1 #@@@@@@@@CHECK THIS!!!!@@@@@@@@@
ah = AtomHybridization()
ah.assignHybridization(lM.allAtoms)
#process the ligand:
#(1)locate specified atom1, atom2 and atom3 SD-CG-CB
#NB: it is assumed that atom3 has exactly 2 bonds
at_names = atom1_atom2_atom3.split('_')
assert len(at_names) == 3
at1Set = lM.allAtoms.get(at_names[0])
if not len(at1Set):
msg = at_names[0] + " is not in " + ligand_filename
raise msg
at1 = at1Set[0] #SD, closest to ligand, farthest from receptor
if verbose:
print "first ligand atom to superimpose is %s" % (at1.full_name())
at2Set = lM.allAtoms.get(at_names[1])
if not len(at2Set):
def setAutoDockElements(self,
mol,
typeAtoms=0,
reassign=False,
splitAcceptors=False):
if os.path.splitext(
mol.parser.filename)[-1] == '.pdbqt' and reassign is False:
if self.verbose:
print 'setAutoDockElements unnecessary:\n', mol.name, ' already has AD4 atomtypes: not reassigned!'
return
#check that the types have already been set, first
if self.set_aromatic_carbons:
#this sets the autodock_element for the planar cyclic carbons to 'A'
aromatic_carbons = self.acm.setAromaticCarbons(mol)
d = {}
ah = AtomHybridization()
if not len(mol.allAtoms.bonds[0]):
mol.buildBondsByDistance()
ats_with_babel_type = filter(lambda x: hasattr(x, 'babel_type'),
mol.allAtoms)
if typeAtoms or len(ats_with_babel_type) != len(mol.allAtoms):
if self.verbose:
print "assigning babel_types"
ah = AtomHybridization()
ah.assignHybridization(mol.allAtoms)
for item in mol.allAtoms:
if not hasattr(item, 'autodock_element'):
#item.element = item.element.upper()
item.autodock_element = item.element
if item.element == 'H':
if len(item.bonds):
n = item.bonds[0].neighborAtom(item)
if n.element not in ['C', 'A']:
item.autodock_element = 'HD'
else:
#note: if there are no bonds, assume HD
item.autodock_element = 'HD'
elif item.element == 'N':
#this has already been done at beginning of for loop
#if item.babel_type in ['N3+','Ntr', 'Nox']:
# item.autodock_element = 'N'
if item.babel_type in ['N3', 'N2', 'N1']:
item.autodock_element = item.element + 'A'
elif item.babel_type in ['Nam', 'Npl', 'Ng+']:
if len(item.bonds) == 2:
item.autodock_element = item.element + 'A'
elif item.element == 'O':
item.autodock_element = item.element + 'A'
elif item.element == 'S':
#possible sulphur babel_types->['S3+','S3','S2','Sac','Sox','S']
if item.babel_type not in ['Sox', 'Sac']:
item.autodock_element = item.element + 'A'
elif item.element == 'C':
if item.parent.type + '_' + item.name in self.pep_aromList:
item.autodock_element = 'A'
if self.renameAtoms: #
if len(item.name) == 1:
item.name = 'A'
else:
item.name = 'A' + item.name[1:]
elif hasattr(item, 'autodock_element'):
item.autodock_element = item.autodock_element
if splitAcceptors and item.autodock_element in self.acceptorList:
#if item has a bond to a hydrogen:
# change acceptor type 'XA' to 'XB' for 'B'oth 'A'cceptor and 'D'onor
if 'H' in item.bonds.getAtoms().element:
#O->OB;N->NB;S->SB
item.autodock_element = item.element + 'B'
d[item.autodock_element] = 1
type_list = d.keys()
type_list.sort()
mol.types = type_list
def addHydrogens(self, mol):
#check for bonds
if len(mol.allAtoms.bonds[0])==0:
mol.buildBondsByDistance()
bonds = mol.allAtoms.bonds[0]
#could have preset babel_types
#so check if allAtoms are already typed
try:
t = mol.allAtoms.babel_type
except:
#if all are not pretyped, type them
babel = AtomHybridization()
babel.assignHybridization(mol.allAtoms)
if self.method=='withBondOrder':
mol.rings = RingFinder()
mol.rings.findRings2(mol.allAtoms, mol.allAtoms.bonds[0])
mol.rings.bondRings = {}
for ind in xrange(len(mol.rings.rings)):
r = mol.rings.rings[ind]
for b in r['bonds']:
if not mol.rings.bondRings.has_key(b):
mol.rings.bondRings[b] = [ind,]
else:
mol.rings.bondRings[b].append(ind)
bo = BondOrder()
bo.assignBondOrder(mol.allAtoms, bonds, mol.rings)
mol.allAtoms._bndtyped = 1
# do aromatic here
arom = Aromatic(mol.rings)
arom.find_aromatic_atoms(mol.allAtoms)
hat = AddHydrogens().addHydrogens(mol.allAtoms, method=self.method)
bondedAtomDict = {} # key is heavy atom
for a in hat:
if bondedAtomDict.has_key(a[1]):
bondedAtomDict[a[1]].append(a)
else:
bondedAtomDict[a[1]] = [a]
# now create Atom object for hydrogens
# and add the to the residues's atom list
molNewHs = AtomSet([]) # list of created H atoms for this molecule
heavyAtoms = AtomSet([]) # list of atoms that need new radii
for heavyAtom, HatmsDscr in bondedAtomDict.items():
#don't add hydrogens to carbons: polar Only!!!
if self.htype!='all' and heavyAtom.element=='C':
continue
res = heavyAtom.parent
# find where to insert H atom
childIndex = res.children.index(heavyAtom)+1
# loop over H atoms description to be added
# start at the end to number correctly
l = len(HatmsDscr)
for i in range(l-1,-1,-1):
a = HatmsDscr[i]
# build H atom's name
if len(heavyAtom.name)==1:
name = 'H' + heavyAtom.name
else:
name = 'H' + heavyAtom.name[1:]
# if more than 1 H atom, add H atom index
# for instance HD11, HD12, Hd13 (index is 1,2,3)
if l > 1:
name = name + str(i+1)
# create the H atom object
atom = Atom(name, res, top=heavyAtom.top,
chemicalElement='H',
childIndex=childIndex, assignUniqIndex=0)
# set atoms attributes
atom._coords = [ a[0] ]
if hasattr(a[1], 'segID'): atom.segID = a[1].segID
atom.hetatm = 0
atom.alternate = []
#atom.element = 'H'
atom.occupancy = 1.0
atom.conformation = 0
atom.temperatureFactor = 0.0
atom.babel_atomic_number = a[2]
atom.babel_type = a[3]
atom.babel_organic = 1
atom.radius = 1.2
# create the Bond object bonding Hatom to heavyAtom
bond = Bond( a[1], atom, bondOrder=1)
# add the created atom the the list
molNewHs.append(atom)
# in case this new hydrogen atom ever ends up in pmv
# HAVE TO CREATE THESE ENTRIES
# create the color entries for all geoemtries
# available for the heavyAtom
for key, value in heavyAtom.colors.items():
atom.colors[key]=(0.0, 1.0, 1.0)
atom.opacities[key]=1.0
mol.allAtoms = mol.chains.residues.atoms
if self.renumber:
mol.allAtoms.number = range(1, len(mol.allAtoms)+1)
return len(molNewHs)
if not len(resPSet):
msg= resP.name + " is not a residue in " + receptor_filename
raise msg
if len(resPSet)>1:
msg= resP.name + " specifies more than one residue:" + resP.full_name()
raise msg
resP = resPSet[0]
if verbose: print "receptor residue is %s which has %d atoms" %(resP.full_name(), len(resP.atoms))
#initialize the ligand
lM = Read(ligand_filename)[0]
if verbose: print 'read ', ligand_filename
lM.buildBondsByDistance() # try to assign bond order;set to 1 if exception
#lM.allAtoms.bonds[0].bondOrder = 1 #@@@@@@@@CHECK THIS!!!!@@@@@@@@@
ah = AtomHybridization()
ah.assignHybridization(lM.allAtoms)
#process the ligand:
#(1)locate specified atom1, atom2 and atom3 SD-CG-CB
#NB: it is assumed that atom3 has exactly 2 bonds
at_names = atom1_atom2_atom3.split('_')
assert len(at_names)==3
at1Set = lM.allAtoms.get(at_names[0])
if not len(at1Set):
msg= at_names[0] + " is not in " + ligand_filename
raise msg
at1 = at1Set[0] #SD, closest to ligand, farthest from receptor
if verbose: print "first ligand atom to superimpose is %s" %(at1.full_name())
at2Set = lM.allAtoms.get(at_names[1])
if not len(at2Set):
msg = at_names[1] + " is not in " + ligand_filename
def getHBAtoms(mol):
"""
Function to identify donor and acceptor atoms for hydrogen bonds
d2, d3, a2, a3 <- getHBAtoms(mol)
The function will first build bonds then assign atom hybridization
and bond orders. Next it will use a HydrogenBondBuilder to identify and'
report donor and acceptor atoms in sets corresponding to Sp2 and Sp3
hybridization.
A .hbstatus is added to all atoms. The value can be:
NE: NEutral
D2: Sp2 donor
D3: Sp3 donor
A2: Sp2 acceptor
A3: Sp3 acceptor
B2: Sp2 acceptor and donor
B3: Sp3 acceptor and donor
"""
# add bonds
mol.buildBondsByDistance()
atoms = mol.allAtoms
# assign .babel_type
from PyBabel.atomTypes import AtomHybridization
atyper = AtomHybridization()
atyper.assignHybridization(atoms)
# assign bond order
from PyBabel.bo import BondOrder
bond_orderer = BondOrder()
bond_orderer.assignBondOrder(atoms, atoms.bonds[0])
# get donors
hbbuilder = HydrogenBondBuilder()
donorTypes = hbbuilder.paramDict['donorTypes']
donorsp2Ats, donorsp3Ats = hbbuilder.getHBDonors(atoms, donorTypes)
# get acceptors
acceptorTypes = hbbuilder.paramDict['acceptorTypes']
acceptorsp2Ats, acceptorsp3Ats = hbbuilder.getHBAcceptors(
atoms, acceptorTypes)
# create hbstatus attribute
atoms.hbstatus = 'NE'
for a in donorsp2Ats:
a.hbstatus = 'D2'
for a in donorsp3Ats:
a.hbstatus = 'D3'
for a in acceptorsp2Ats:
a.hbstatus = 'A2'
for a in acceptorsp3Ats:
a.hbstatus = 'A3'
# handle atoms that are both donors and acceptor
for a in donorsp2Ats.inter(acceptorsp2Ats):
a.hbstatus = 'B2'
for a in donorsp3Ats.inter(acceptorsp3Ats):
a.hbstatus = 'B3'
return donorsp2Ats, donorsp3Ats, acceptorsp2Ats, acceptorsp3Ats
def add_oxt(self, catom):
if catom.element!='C':
return
mol = catom.top
##check for bonds
#if len(mol.allAtoms.bonds[0])==0:
# mol.buildBondsByDistance()
#check whether residue already has OXT
res = catom.parent
if 'OXT' in res.atoms.name:
print 'not adding OXT to ',res.full_name(),'\n', 'it already has an OXT atom'
return
#check whether catom has a hydrogen to delete
hatoms = catom.parent.atoms.get(lambda x: x.name=='HC')
if len(hatoms):
hatom = hatoms[0]
#check for hbonds
if hasattr(hatom, 'hbonds'):
#remove hbonds
for b in hatom.hbonds:
atList = [b.donAt, b.accAt]
if b.hAt is not None:
atList.append(b.hAt)
for at in atList:
#hbonds might already be gone
if not hasattr(at, 'hbonds'):
continue
okhbnds = []
for hb in at.hbonds:
if hb!=b:
okhbnds.append(hb)
if len(okhbnds):
at.hbonds = okhbnds
else:
delattr(at, 'hbonds')
#remove covalent bonds
for b in hatom.bonds:
at2 = b.atom1
if at2 == hatom: at2 = b.atom2
at2.bonds.remove(b)
hatom.parent.remove(hatom, cleanup=1)
#have to type atoms before call to add_sp2_hydrogen:
if not hasattr(catom,'babel_type'):
print 'catom has no babel_type: calling typeAtoms'
#self.warningMsg(msg)
#typeAtoms does whole molecule
babel = AtomHybridization()
babel.assignHybridization(mol.allAtoms)
#NB: bond_length 1.28 measured from OXT-C bond in 1crn
tup1 = self.addh.add_sp2_hydrogen(catom, 1.28)
res = catom.parent
# find where to insert H atom
childIndex = res.children.index(catom)+1
name = 'OXT'
# create the OXT atom object
atom = Atom(name, res, top=mol,
childIndex=childIndex, assignUniqIndex=0)
# set atoms attributes
atom._coords = [ tup1[0][0] ]
if hasattr(catom, 'segID'): atom.segID = catom.segID
atom.hetatm = 0
atom.alternate = []
atom.element = 'O'
atom.occupancy = 1.0
atom.conformation = 0
atom.temperatureFactor = 0.0
atom.babel_atomic_number = 8
atom.babel_type = 'O-'
atom.babel_organic = 1
# create the Bond object bonding Hatom to heavyAtom
bond = Bond( catom, atom, bondOrder=2)
# create the color entries for all geometries
# available for the other oxygen atom attached to 'C'
oatom = res.atoms.get(lambda x: x.name=='O')[0]
if oatom is not None:
for key, value in oatom.colors.items():
atom.colors[key] = value
#atom.opacities[key] = oatom.opacities[key]
# update the allAtoms set in the molecule
mol.allAtoms = mol.chains.residues.atoms
# update numbers of allAtoms
fst = mol.allAtoms[0].number
mol.allAtoms.number = range(fst, len(mol.allAtoms)+fst)
# update _uniqIndex of this residues atoms
res.assignUniqIndex()
#return AtomSet([atom])
return atom