def testOBMolSeparatePreservesAtomOrder(self):
"""Originally Separate() preserved DFS order rather
than atom order"""
# First test
smi = "C123.F3.Cl2.Br1"
mol = pybel.readstring("smi", smi)
atomicnums = [atom.OBAtom.GetAtomicNum() for atom in mol]
mols = mol.OBMol.Separate()
new_atomicnums = [
atom.OBAtom.GetAtomicNum() for atom in pybel.Molecule(mols[0])
]
for x, y in zip(atomicnums, new_atomicnums):
self.assertEqual(x,
y) # check that the atoms have not been permuted
# Second test
xyz = """6
examples/water_dimer.xyz
O 0.12908 -0.26336 0.64798
H 0.89795 0.28805 0.85518
H 0.10833 -0.20468 -0.33302
O 0.31020 0.07569 -2.07524
H 0.64083 -0.57862 -2.71449
H -0.26065 0.64232 -2.62218
"""
mol = pybel.readstring("xyz", xyz)
mols = mol.OBMol.Separate()
allatoms = pybel.Molecule(mols[0]).atoms + pybel.Molecule(
mols[1]).atoms
for idx, atom in enumerate(allatoms):
xcoord = atom.OBAtom.GetX()
orig_xcoord = mol.OBMol.GetAtom(idx + 1).GetX()
self.assertEqual(xcoord, orig_xcoord)
def test_rb_basic():
# DNM
mol = calc_props.smiles_to_ob("CC(C1=CC(C(C)=CC(N2C)=O)=C2C3=C1N4CO3)=CC4=O")
pymol = pybel.Molecule(mol)
assert_equals(calc_props.rotatable_bonds(pymol), 0)
# Ribocil C
mol = calc_props.smiles_to_ob("C1CC(CN(C1)CC2=CN(C=N2)C3=NC=CC=N3)C4=NC(=O)C=C(N4)C5=CC=CS5")
pymol = pybel.Molecule(mol)
assert_equals(calc_props.rotatable_bonds(pymol), 5)
# Triphenylphosphine
mol = calc_props.smiles_to_ob("C1(P(C2=CC=CC=C2)C3=CC=CC=C3)=CC=CC=C1")
pymol = pybel.Molecule(mol)
assert_equals(calc_props.rotatable_bonds(pymol), 3)
def testBondOrders(self):
mol = pybel.readstring("smi", "O=C=O")
bv = self.createBitVec(3, (2, 3))
bondbv = self.createBitVec(2, (1,))
ans = ["[C].[O]", "C.O", "C(=*)=*.O=*"]
for option in range(3):
nmol = ob.OBMol()
ok = mol.OBMol.CopySubstructure(nmol, bv, bondbv, option)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), ans[option])
ans = ["[C]=O", "C=O", "C(=O)=*"]
for option in range(3):
nmol = ob.OBMol()
ok = mol.OBMol.CopySubstructure(nmol, bv, None, option)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), ans[option])
def _write_input(self, input_dir="."):
"""
Write the packmol input file to the input directory.
Args:
input_dir (string): path to the input directory
"""
with open(os.path.join(input_dir, self.input_file), "wt", encoding="utf-8") as inp:
for k, v in self.control_params.items():
inp.write(f"{k} {self._format_param_val(v)}\n")
# write the structures of the constituent molecules to file and set
# the molecule id and the corresponding filename in the packmol
# input file.
for idx, mol in enumerate(self.mols):
filename = os.path.join(input_dir, f"{idx}.{self.control_params['filetype']}")
# pdb
if self.control_params["filetype"] == "pdb":
self.write_pdb(mol, filename, num=idx + 1)
# all other filetypes
else:
a = BabelMolAdaptor(mol)
pm = pb.Molecule(a.openbabel_mol)
pm.write(
self.control_params["filetype"],
filename=filename,
overwrite=True,
)
inp.write("\n")
inp.write(f"structure {os.path.join(input_dir, str(idx))}.{self.control_params['filetype']}\n")
for k, v in self.param_list[idx].items():
inp.write(f" {k} {self._format_param_val(v)}\n")
inp.write("end structure\n")
def xyz_to_pyMol(xyz, cluster_bond_path=None):
mol = next(pybel.readfile('xyz', xyz))
if cluster_bond_path:
m = pybel.ob.OBMol()
m.BeginModify()
for atom in mol:
coords = [coord for coord in atom.coords]
atomno = atom.atomicnum
obatom = ob.OBAtom()
obatom.thisown = 0
obatom.SetAtomicNum(atomno)
obatom.SetVector(*coords)
m.AddAtom(obatom)
del obatom
with open(cluster_bond_path, 'r') as f:
lines = f.read()
cluster_bond = eval(lines)
bonds = [(bond.GetBeginAtomIdx(), bond.GetEndAtomIdx(),
bond.GetBondOrder())
for bond in pybel.ob.OBMolBondIter(mol.OBMol)]
bonds.extend(cluster_bond)
for bond in bonds:
m.AddBond(bond[0], bond[1], bond[2])
pybelmol = pybel.Molecule(m)
return pybelmol
else:
return mol
def testStereo(self):
data = [
("FC[C@@](Br)(Cl)I", [((2, 3, 4, 5, 6), None, "C[C@@](Br)(Cl)I"),
((2, 3, 4, 5), None, "CC(Br)Cl"),
((1, 2, 3, 4, 5, 6), (4, ), "FCC(Br)Cl.I")]),
("[C@@H](Br)(Cl)I", [((1, 2, 3), None, "C(Br)Cl"),
((1, 2, 3, 4), (2, ), "C(Br)Cl.I")]),
("C[C@@H]1CO1", [
((2, 3, 4), None, "C1CO1"),
]),
("F/C=C/I", [((1, 2, 3, 4), None, "F/C=C/I"),
((1, 2, 3), None, "FC=C"),
((1, 2, 3, 4), (0, ), "F.C=CI"),
((1, 2, 3, 4), (1, ), "FC.CI")]),
]
for smi, d in data:
mol = pybel.readstring("smi", smi)
for a, b, ans in d:
nmol = ob.OBMol()
bv = self.createBitVec(7, a)
bondbv = None if b is None else self.createBitVec(5, b)
ok = mol.OBMol.CopySubstructure(nmol, bv, bondbv)
self.assertTrue(ok)
if "@" not in ans and "/" not in ans:
self.assertFalse(nmol.GetData(ob.StereoData))
self.assertEqual(
pybel.Molecule(nmol).write("smi").rstrip(), ans)
def canonicalize(lig, preserve_bond_order=False):
"""Get the canonical atom order for the ligand."""
atomorder = None
# Get canonical atom order
lig = pybel.ob.OBMol(lig.OBMol)
if not preserve_bond_order:
for bond in pybel.ob.OBMolBondIter(lig):
if bond.GetBondOrder() != 1:
bond.SetBondOrder(1)
lig.DeleteData(pybel.ob.StereoData)
lig = pybel.Molecule(lig)
testcan = lig.write(format='can')
try:
pybel.readstring('can', testcan)
reference = pybel.readstring('can', testcan)
except IOError:
testcan, reference = '', ''
if testcan != '':
reference.removeh()
isomorphs = get_isomorphisms(
reference,
lig) # isomorphs now holds all isomorphisms within the molecule
if not len(isomorphs) == 0:
smi_dict = {}
smi_to_can = isomorphs[0]
for x in smi_to_can:
smi_dict[int(x[1]) + 1] = int(x[0]) + 1
atomorder = [smi_dict[x + 1] for x in range(len(lig.atoms))]
else:
atomorder = None
return atomorder
def testAtomMapsAfterCopying(self):
"""Copying a molecule should copy the atom maps"""
smi = "C[CH2:2]O[Cl:6]"
obmol = pybel.readstring("smi", smi).OBMol
copy = pybel.ob.OBMol(obmol)
copysmi = pybel.Molecule(copy).write("smi", opt={"a": True})
self.assertEqual(copysmi.rstrip(), smi)
def restore_site_properties(self, site_property="ff_map", filename=None):
"""
Restore the site properties for the final packed molecule.
Args:
site_property (str):
filename (str): path to the final packed molecule.
Returns:
Molecule
"""
# only for pdb
if not self.control_params["filetype"] == "pdb":
raise ValueError()
filename = filename or self.control_params["output"]
bma = BabelMolAdaptor.from_file(filename, "pdb")
pbm = pb.Molecule(bma._obmol)
assert len(pbm.residues) == sum(x["number"] for x in self.param_list)
packed_mol = self.convert_obatoms_to_molecule(
pbm.residues[0].atoms,
residue_name=pbm.residues[0].name,
site_property=site_property,
)
for resid in pbm.residues[1:]:
mol = self.convert_obatoms_to_molecule(resid.atoms, residue_name=resid.name, site_property=site_property)
for site in mol:
packed_mol.append(site.species, site.coords, properties=site.properties)
return packed_mol
def add_hydrogen(self):
from openbabel import pybel as pb
mol_0d = pb.readstring("smi", "CCCC").OBMol
self.assertEqual(len(pb.Molecule(mol_0d).atoms), 2)
adaptor = BabelMolAdaptor(mol_0d)
adaptor.add_hydrogen()
self.assertEqual(len(adaptor.pymatgen_mol.sites), 14)
def test_glob():
obmol = openbabel.OBMol()
obConv = openbabel.OBConversion()
obConv.SetInFormat("mol")
obConv.ReadFile(obmol, os.path.join(THIS_DIR, "data/triphenylphosphine.mol"))
pymol = pybel.Molecule(obmol)
points = calc_props.get_atom_coords(pymol)
assert_almost_equal(calc_props.calc_glob(points), 0.245503, 6, 1)
def json_to_pybel(data):
"""Converts a python data structure to pybel.Molecule.
The data structure is a plain python object of the form:
```
{
"atoms": [{"location": [0, 0, 0], "element": "H", "label": "H1",
"charge": 0}, ...],
"bonds": [{"source": 0, "target": 0, "order": 1}, ...],
"unitcell": [[0, 0, 0], [0, 0, 0], [0, 0, 0]]
}
```
It is referred to as "json" because this data structure is intended to
be read from and written to json files or databases.
As RASPA makes no use of bond information, this field is ignored.
The labels are stripped and replaced with "MOF_{element}", in accordance
with the CrystalGenerator forcefield notation. Therefore, labels are also
ignored.
Args:
data: the molecule, as a python object
Returns:
An instance of `pybel.Molecule`
"""
if not PYBEL_LOADED:
raise ImportError("Open Babel not installed.")
if "building_blocks" in data:
data["atoms"] = [
a for bb in data["building_blocks"] for a in bb["atoms"]
]
obmol = pybel.ob.OBMol()
obmol.BeginModify()
for atom in data["atoms"]:
obatom = obmol.NewAtom()
obatom.SetAtomicNum(GetAtomicNum(str(atom["element"])))
obatom.SetVector(*atom["location"])
uc = pybel.ob.OBUnitCell()
uc.SetData(*(pybel.ob.vector3(*v) for v in data["unitcell"]))
uc.SetSpaceGroup("P1")
obmol.CloneData(uc)
obmol.EndModify()
mol = pybel.Molecule(obmol)
# Add partial charges
if "charge" in data["atoms"][0]:
mol.OBMol.SetPartialChargesPerceived()
for atom, pyatom in zip(data["atoms"], mol.atoms):
pyatom.OBAtom.SetPartialCharge(atom["charge"])
return mol
def testBasic(self):
mol = pybel.readstring("smi", "ICBr")
bv = self.createBitVec(4, (1, 3))
nmol = ob.OBMol()
ok = mol.OBMol.CopySubstructure(nmol, bv, None, 0)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), "[I].[Br]")
bv = self.createBitVec(4, (2,))
ok = mol.OBMol.CopySubstructure(nmol, bv, None, 0)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), "[I].[Br].[CH2]")
mol = pybel.readstring("smi", "CCC")
bv = self.createBitVec(4, (1,))
bondv = self.createBitVec(2, (1,))
nmol = ob.OBMol()
ok = mol.OBMol.CopySubstructure(nmol, bv, bondv, 0)
self.assertTrue(ok)
def testResidueCopying(self):
smi = "C[C@@H](C(=O)N[C@@H](CS)C(=O)O)N" # H-Ala-Cys-OH
mol = pybel.readstring("smi", smi).OBMol
ob.cvar.chainsparser.PerceiveChains(mol)
mol.SetChainsPerceived()
residues = list(ob.OBResidueIter(mol))
self.assertEqual(len(residues), 2)
# Copy just the Cys N
bv = self.createBitVec(mol.NumAtoms() + 1, (5, ))
nmol = ob.OBMol()
mol.CopySubstructure(nmol, bv)
self.assertEqual(len(list(ob.OBResidueIter(nmol))), 1)
pdb = pybel.Molecule(nmol).write("pdb")
atoms = [line for line in pdb.split("\n") if line.startswith("ATOM")]
self.assertEqual(len(atoms), 1)
cysN = "ATOM 1 N CYS A 2"
self.assertTrue(atoms[0].startswith(cysN))
# Copy the Cys N and Ca
bv = self.createBitVec(mol.NumAtoms() + 1, (5, 6))
nmol.Clear()
mol.CopySubstructure(nmol, bv)
self.assertEqual(len(list(ob.OBResidueIter(nmol))), 1)
pdb = pybel.Molecule(nmol).write("pdb")
atoms = [line for line in pdb.split("\n") if line.startswith("ATOM")]
self.assertEqual(len(atoms), 2)
self.assertTrue(atoms[0].startswith(cysN))
cysCa = "ATOM 2 CA CYS A 2"
self.assertTrue(atoms[1].startswith(cysCa))
# Copy the Ala C and Cys N
bv = self.createBitVec(mol.NumAtoms() + 1, (3, 5))
nmol.Clear()
mol.CopySubstructure(nmol, bv)
self.assertEqual(len(list(ob.OBResidueIter(nmol))), 2)
pdb = pybel.Molecule(nmol).write("pdb")
atoms = [line for line in pdb.split("\n") if line.startswith("ATOM")]
self.assertEqual(len(atoms), 2)
alaC = "ATOM 1 C ALA A 1"
self.assertTrue(atoms[0].startswith(alaC))
cysN = "ATOM 2 N CYS A 2"
self.assertTrue(atoms[1].startswith(cysN))
def write_file(self, filename, file_format="xyz"):
"""
Uses OpenBabel to output all supported formats.
Args:
filename: Filename of file to output
file_format: String specifying any OpenBabel supported formats.
"""
mol = pb.Molecule(self._obmol)
return mol.write(file_format, filename, overwrite=True)
def testLeaveUnchanged(self):
data = [
"CC[N+](=O)[O-]", # nitro
"c1ccc[n+]([O-])c1", # pyridine N-oxide
"C1=NC(=O)NC(=O)C1=[N+]=N", # diazenium
]
for smi in data:
mol = pybel.readstring("smi", smi).OBMol
neutralize(mol)
self.assertEqual(smi, pybel.Molecule(mol).write("smi").rstrip())
def testSpecifyAtomsAndBonds(self):
# Now copy just a subset of atoms too
mol = pybel.readstring("smi", "ICBr")
bv = self.createBitVec(4, (1, 3))
bondbv = self.createBitVec(2, (1,))
ans = ["[I].[Br]", "I.Br", "I*.Br*"]
for option in range(3):
nmol = ob.OBMol()
ok = mol.OBMol.CopySubstructure(nmol, bv, bondbv, option)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), ans[option])
def json_to_pybel(data, infer_bonds=False):
"""Converts python data structure to pybel.Molecule.
This will infer bond data if not specified.
Args:
data: The loaded json data of a molecule, as a Python object
infer_bonds (Optional): If no bonds specified in input, infer them
Returns:
An instance of `pybel.Molecule`
"""
obmol = ob.OBMol()
obmol.BeginModify()
for atom in data['atoms']:
obatom = obmol.NewAtom()
obatom.SetAtomicNum(table.GetAtomicNum(str(atom['element'])))
obatom.SetVector(*atom['location'])
if 'label' in atom:
pd = ob.OBPairData()
pd.SetAttribute('_atom_site_label')
pd.SetValue(atom['label'])
obatom.CloneData(pd)
# If there is no bond data, try to infer them
if 'bonds' not in data or not data['bonds']:
if infer_bonds:
obmol.ConnectTheDots()
obmol.PerceiveBondOrders()
# Otherwise, use the bonds in the data set
else:
for bond in data['bonds']:
if 'atoms' not in bond:
continue
obmol.AddBond(bond['atoms'][0] + 1, bond['atoms'][1] + 1,
bond['order'])
# Check for unit cell data
if 'unitcell' in data:
uc = ob.OBUnitCell()
uc.SetData(*(ob.vector3(*v) for v in data['unitcell']))
uc.SetSpaceGroup('P1')
obmol.CloneData(uc)
obmol.EndModify()
mol = pybel.Molecule(obmol)
# Add partial charges
if 'charge' in data['atoms'][0]:
mol.OBMol.SetPartialChargesPerceived()
for atom, pyatom in zip(data['atoms'], mol.atoms):
pyatom.OBAtom.SetPartialCharge(atom['charge'])
return mol
def localopt(self, forcefield='mmff94', steps=500):
"""
A wrapper to pybel's localopt method to optimize a Molecule.
Args:
forcefield: Default is mmff94. Options are 'gaff', 'ghemical',
'mmff94', 'mmff94s', and 'uff'.
steps: Default is 500.
"""
pbmol = pb.Molecule(self._obmol)
pbmol.localopt(forcefield=forcefield, steps=steps)
self._obmol = pbmol.OBMol
def testFacade(self):
parts = "CNO"
mol = pybel.readstring("smi", ">".join(parts)).OBMol
facade = ob.OBReactionFacade(mol)
# basic test - copy out each component
comps = [ob.REACTANT, ob.AGENT, ob.PRODUCT]
for part, comp in zip(parts, comps):
nmol = ob.OBMol()
facade.GetComponent(nmol, comp, 0)
nsmi = pybel.Molecule(nmol).write("smi").rstrip()
self.assertEqual(nsmi, part)
nmol = ob.OBMol()
facade.GetComponent(nmol, ob.NO_REACTIONROLE, 0)
self.assertEqual(0, nmol.NumAtoms())
# Reassign role
facade.ReassignComponent(ob.AGENT, 0, ob.NO_REACTIONROLE)
nsmi = pybel.Molecule(mol).write("smi").rstrip()
self.assertEqual("C>>O", nsmi)
# ...and back again
facade.ReassignComponent(ob.NO_REACTIONROLE, 0, ob.AGENT)
# Add a new reactant
molb = pybel.readstring("smi", "S").OBMol
facade.AddComponent(molb, ob.REACTANT)
nsmi = pybel.Molecule(mol).write("smi").rstrip()
self.assertEqual("C.S>N>O", nsmi)
# ...and copy it back out
nmol = ob.OBMol()
facade.GetComponent(nmol, ob.REACTANT, 1)
nsmi = pybel.Molecule(nmol).write("smi").rstrip()
self.assertEqual("S", nsmi)
# ...and also copy the O
facade.GetComponent(nmol, ob.PRODUCT, 0)
nmol.SetIsReaction()
nsmi = pybel.Molecule(nmol).write("smi").rstrip()
self.assertEqual("S>>O", nsmi)
def draw(self, conformer_num=0, ipython_3d=True) -> None:
"""Draw a depiction of the molecule for a given conformer.
:param conformer_num: conformer number, if larger than number of conformations available, the last is returned
:param ipython_3d: if True 3-dim rotatable graphics is generated
"""
self.mol.SetConformer(conformer_num)
pybel.ipython_3d = ipython_3d
try:
from IPython.core.display import display
display(pybel.Molecule(self.mol))
except ImportError as e:
logger.warning(f"Import Error: {e}")
def generate_inter_lp(init_str: pybel.Molecule, end_str: pybel.Molecule, inter: int):
int_list = [pybel.Molecule(ob.OBMol()) for i in range(inter)]
for i, j in zip(init_str.atoms, end_str.atoms):
# define the vector for propagation
i_coord = np.array(i.coords)
j_coord = np.array(j.coords)
coord_vector = (j_coord - i_coord) / (inter + 1)
for k in range(inter):
# define the atomic position for k-th intermediate and write to OBmol object
atom_position = i_coord + coord_vector * (k + 1)
newatom = ob.OBAtom()
newatom.SetAtomicNum(i.OBAtom.GetAtomicNum())
newatom.SetVector(atom_position[0], atom_position[1], atom_position[2])
int_list[k].OBMol.AddAtom(newatom)
return int_list
def testOptions(self):
mol = pybel.readstring("smi", "ICBr")
bv = self.createBitVec(4, (1, 3))
ans = ["[I].[Br]", "I.Br", "I*.Br*"]
ans_atomorder = [[1, 3], [1, 3], [1, 3, 2, 2]]
ans_bondorder = [ [], [], [0, 1] ]
for option in range(3):
nmol = ob.OBMol()
atomorder = ob.vectorUnsignedInt()
bondorder = ob.vectorUnsignedInt()
ok = mol.OBMol.CopySubstructure(nmol, bv, None, option, atomorder, bondorder)
self.assertTrue(ok)
self.assertEqual(pybel.Molecule(nmol).write("smi").rstrip(), ans[option])
self.assertEqual(ans_atomorder[option], list(atomorder))
self.assertEqual(ans_bondorder[option], list(bondorder))
def pybel_opt(smile, steps):
obconversion = ob.OBConversion()
obconversion.SetInFormat('smi')
obmol = ob.OBMol()
obconversion.ReadString(obmol, smile)
pbmol = pb.Molecule(obmol)
pbmol.make3D(forcefield="uff", steps=50)
pbmol.localopt(forcefield="gaff", steps=200)
pbmol.localopt(forcefield="mmff94", steps=100)
f_f = pb._forcefields["uff"]
f_f.Setup(pbmol.OBMol)
f_f.ConjugateGradients(steps, 1.0e-9)
f_f.GetCoordinates(pbmol.OBMol)
#print(f_f.Energy(), f_f.GetUnit())
return pybel2ase(pbmol)
def runvina(infile, outfile, receptor, tmp_file='test.pdbqt', vina=None):
obconversion = OBConversion()
obconversion.SetInFormat("sdf")
obconversion.SetOutFormat("pdbqt")
obmol = OBMol()
notatend = obconversion.ReadFile(obmol, infile)
obmol2 = OBMol(obmol)
ofs = pybel.Outputfile("sdf", outfile, overwrite=True)
pbar = tqdm()
while notatend:
pbar.update(1)
if obconversion.WriteFile(obmol, tmp_file):
try:
x = subprocess.check_output([
vina, "--score_only", "--receptor", receptor, "--ligand",
tmp_file
],
shell=False)
# x2 = subprocess.check_output(["/Users/austin/Downloads/rf-score-4/rf-score", "/Users/austin/Downloads/rf-score-4/pdbbind-2014-refined.rf", receptor, tmp_file])
# print(x2)
mol2 = pybel.Molecule(obmol2)
mol2.data.update({'AutodockVinaRescoreOnly': str(get_aff(x))})
ofs.write(mol2)
except subprocess.CalledProcessError as e:
print(e)
ofs.write(obmol)
except ValueError as e:
print(e)
ofs.write(obmol)
else:
print("error writing")
obmol = OBMol()
notatend = obconversion.Read(obmol)
obmol2 = OBMol(obmol)
pbar.close()
print("FAILED")
def _make_openbabel_from_ccdata(self):
"""Create Open Babel and Pybel molecules from ccData."""
if not hasattr(self.ccdata, 'charge'):
logging.warning("ccdata object does not have charge, setting to 0")
_charge = 0
else:
_charge = self.ccdata.charge
if not hasattr(self.ccdata, 'mult'):
logging.warning(
"ccdata object does not have spin multiplicity, setting to 1")
_mult = 1
else:
_mult = self.ccdata.mult
obmol = makeopenbabel(self.ccdata.atomcoords,
self.ccdata.atomnos,
charge=_charge,
mult=_mult)
if self.jobfilename is not None:
obmol.SetTitle(self.jobfilename)
return (obmol, pb.Molecule(obmol))
def atoms_to_pybel(aseatoms, infer_bonds=True):
'''
Convert ASE Atoms isntance into the json format compatible with
Args:
aseatoms : ase.Atoms
Instance of Atoms from ase package
infer_bonds : bool
If `True` bonds will be inferred using openbabel
Returns:
mol : dist
A dictionary with the json format of the molecule
'''
from openbabel import pybel
from openbabel import openbabel as ob
obmol = ob.OBMol()
obmol.BeginModify()
for atom in aseatoms:
obatom = obmol.NewAtom()
obatom.SetAtomicNum(int(atom.number))
obatom.SetVector(*atom.position.tolist())
# If there is no bond data, try to infer them
if infer_bonds:
obmol.ConnectTheDots()
obmol.PerceiveBondOrders()
# Check for unit cell data
if any(aseatoms.pbc):
uc = ob.OBUnitCell()
uc.SetData(*(ob.vector3(*v) for v in aseatoms.get_cell()))
uc.SetSpaceGroup('P1')
obmol.CloneData(uc)
obmol.EndModify()
mol = pybel.Molecule(obmol)
return mol
def _pybel_opt(self, smile, steps):
"""Optimize a molecule using force field and pybel (needed for complex SMILES)."""
obconversion = ob.OBConversion()
obconversion.SetInFormat("smi")
obmol = ob.OBMol()
obconversion.ReadString(obmol, smile)
pbmol = pb.Molecule(obmol)
pbmol.make3D(forcefield="uff", steps=50)
pbmol.localopt(forcefield="gaff", steps=200)
pbmol.localopt(forcefield="mmff94", steps=100)
f_f = pb._forcefields["uff"] # pylint: disable=protected-access
f_f.Setup(pbmol.OBMol)
f_f.ConjugateGradients(steps, 1.0e-9)
f_f.GetCoordinates(pbmol.OBMol)
species = [chemical_symbols[atm.atomicnum] for atm in pbmol.atoms]
positions = np.asarray([atm.coords for atm in pbmol.atoms])
return self.make_ase(species, positions)
def write_pdb(mol, filename, name=None, num=None):
"""
dump the molecule into pdb file with custom residue name and number.
"""
# ugly hack to get around the openbabel issues with inconsistent
# residue labelling.
scratch = tempfile.gettempdir()
with ScratchDir(scratch, copy_to_current_on_exit=False) as _:
mol.to(fmt="pdb", filename="tmp.pdb")
bma = BabelMolAdaptor.from_file("tmp.pdb", "pdb")
num = num or 1
name = name or "ml{}".format(num)
# bma = BabelMolAdaptor(mol)
pbm = pb.Molecule(bma._obmol)
for i, x in enumerate(pbm.residues):
x.OBResidue.SetName(name)
x.OBResidue.SetNum(num)
pbm.write(format="pdb", filename=filename, overwrite=True)
def make3d(self, forcefield="mmff94", steps=50):
"""
A wrapper to pybel's make3D method generate a 3D structure from a
2D or 0D structure.
The 3D structure is made very quickly using a combination of rules
(e.g. sp3 atoms should have four bonds arranged in a tetrahedron) and
ring templates (e.g. cyclohexane is shaped like a chair). Once 3D
coordinates are generated, hydrogens are added and a quick local
optimization is carried out as default.
The generated 3D structure can have clashes or have high energy
structures due to some strain. Please consider to use the conformer
search or geometry optimization to further optimize the structure.
Args:
forcefield: Default is mmff94. Options are 'gaff', 'ghemical',
'mmff94', 'mmff94s', and 'uff'.
steps: Default is 50.
"""
pbmol = pb.Molecule(self._obmol)
pbmol.make3D(forcefield=forcefield, steps=steps)
self._obmol = pbmol.OBMol
