def string(self, val):
if not _os.path.exists(val):
self._molecule = _rdkit.openAsRdkit(val, minimise=self.minimise)
self._string = _rdmolfiles.MolToSmiles(self._molecule)
else:
raise ValueError(
"Need a SMILES or InChI string instead of a filename")
def protonated_filename(self, val):
with self.workdir:
if val is None:
self._protonated_filename = None
self._protonated = False
else:
self._protonated_filename = _fileio.checkFileExists(val)
self._molecule = _rdkit.openAsRdkit(self._protonated_filename,
removeHs=False,
minimise=self.minimise)
self._string = _rdmolfiles.MolToSmiles(self.molecule)
self._protonated = True
def __init__(self,
input,
parametrised_files=None,
name=None,
protonated=False,
minimise=None,
workdir="."):
self.name = name
self.workdir = _fileio.Dir(workdir)
self.minimise = minimise
# always set protonated to False and if a valid protonated file is given it is automatically set to True
self.protonated_filename = None
with self.workdir:
if parametrised_files:
self.molecule = _rdkit.openAsRdkit(parametrised_files,
removeHs=False,
minimise=False,
template=input)
self.protonated_filename = _rdkit.saveFromRdkit(
self.molecule, "{}.pdb".format(name))
elif isinstance(input, str):
if _os.path.exists(input):
if protonated:
self.protonated_filename = input
else:
self.molecule = _rdkit.openAsRdkit(input,
minimise=minimise)
else:
self.string = input
elif isinstance(input, _rdchem.Mol):
self.molecule = input
else:
raise TypeError(
"Need a SMILES, InChI string, filename or an RDKit object as an input"
)
self.parametrised_files = parametrised_files
self.minimise = False
def amberWrapper(params,
filename,
molecule_type,
id=None,
charge=None,
*args,
**kwargs):
"""
Parametrises an input file according to AMBER force field.
Parameters
----------
params : ProtoCaller.Parametrise.Params
Force field parameters.
filename : str
Name of the input file.
molecule_type : str
The type of the molecule. One of: "protein", "ligand", "cofactor", "water", "simple_anion", "complex_anion",
"simple_cation", "complex_cation".
id : str
The name of the molecule. Default: equal to molecule_type.
charge : bool
The net charge of the molecule. Default: automatic detection by antechamber.
args
Positional arguments to be passed to the relevant wrapper.
kwargs
Keyword arguments to be passed to the relevant wrapper.
Returns
-------
files : [str]
The output parametrised file(s). If there is more than one file, the first one is always the topology file and
the second one - the coordinate file.
"""
if id is None: id = molecule_type
force_fields, files, param_files = [], [filename], []
if molecule_type == "protein":
force_fields = [params.protein_ff, params.water_ff]
elif molecule_type in ["water", "simple_anion", "simple_cation"]:
force_fields = [params.water_ff]
elif molecule_type == "complex_anion":
_warnings.warn(
"AMBER parametrisation failed: polyatomic anions not supported")
return
elif molecule_type == "complex_cation":
_warnings.warn(
"AMBER parametrisation failed: transition metals not supported")
return
elif molecule_type == "cofactor":
if params.water_ff != "tip3p" or params.protein_ff != "ff99SB":
_warnings.warn("All cofactors have been parametrised for use with "
"the ff99SB protein force field and the TIP3P "
"water model. Be careful when using these "
"parameters with %s" % params.water_ff.upper())
files = []
force_fields = [params.protein_ff, params.ligand_ff]
param_files = _glob.glob("%s/shared/amber-parameters/cofactors/%s.*" %
(_PC.HOMEDIR, id))
# here we override the default parametrisation behaviour for cofactors
parametrised_files = runTleap(force_fields=force_fields,
files=files,
param_files=param_files,
id=id,
*args,
**kwargs)
filebase = _os.path.splitext(filename)[0]
topol = "{}.prmtop".format(filebase)
_os.rename(parametrised_files[0], topol)
parametrised_files[0] = topol
# convert the parametrised file into PDB and load in RDKit
ref = _rdkit.openAsRdkit(filename, removeHs=False)
mol = _pmd.openFilesAsParmed(parametrised_files)
pdb_file = _pmd.saveFilesFromParmed(mol, [filename], overwrite=True)[0]
mol = _rdkit.openAsRdkit(pdb_file, removeHs=False)
# align the parametrised file to the molecule and overwrite
# previous coordinates
mol, mcs = _stdio.stdout_stderr()(_rdkit.alignTwoMolecules) \
(ref, mol, two_way_matching=True,
mcs_parameters=dict(atomCompare="elements"))
if min(mol.GetNumAtoms(), ref.GetNumAtoms()) != len(mcs):
_warnings.warn("The cofactor {} does not perfectly match the "
"AMBER parameter file. Please check your "
"molecule.".format(id))
_os.remove(parametrised_files[1])
coord = "{}.inpcrd".format(filebase)
parametrised_files[1] = _rdkit.saveFromRdkit(mol, coord)
return parametrised_files
elif molecule_type == "ligand":
force_fields = [params.ligand_ff]
files = [runAntechamber(params.ligand_ff, filename, charge=charge)]
param_files = [runParmchk(params.ligand_ff, files[0])]
else:
raise ValueError("Value %s for molecule_type not supported " %
molecule_type)
return runTleap(force_fields=force_fields,
files=files,
param_files=param_files,
id=id,
*args,
**kwargs)
