Python

Accessing Open Babel with Python

There are two ways to access the Open Babel library using Python:

1. The openbabel module, a direct binding of the Open Babel C++ library, created using the SWIG package.
2. Pybel, a set of convenience functions and classes that simplifies access to the openbabel module. (Only available with OpenBabel >= 2.0.3)

For more examples of using Open Babel from Python, see the developer Python tutorial. If you have any questions or find any problems, please send an email to the openbabel-scripting mailing list.

The openbabel module

The openbabel module provides direct access to the C++ Open Babel library from Python. This binding is generated using the SWIG package and provides access to almost all of the Open Babel interfaces via Python, including the base classes OBMol, OBAtom, OBBond, and OBResidue, as well as the conversion framework OBConversion. As such, essentially any call in the C++ API is available to Python scripts with very little difference in syntax. As a result, the principal documentation is the Open Babel C++ API documentation.

Examples

Here we give some examples of common Python syntax for the openbabel module and pointers to the appropriate sections of the API documentation.

The example script below creates atoms and bonds one-by-one using the OBMol, OBAtom, and OBBond classes.

 import openbabel

 mol = openbabel.OBMol()
 print 'Should print 0 (atoms)'
 print mol.NumAtoms()

 a = mol.NewAtom()
 a.SetAtomicNum(6)   # carbon atom
 a.SetVector(0.0, 1.0, 2.0) # coordinates

 b = mol.NewAtom()
 mol.AddBond(1, 2, 1)   # atoms indexed from 1
 print 'Should print 2 (atoms)'
 print mol.NumAtoms()
 print 'Should print 1 (bond)'
 print mol.NumBonds()

 mol.Clear();

More commonly, Open Babel can be used to read in molecules using the OBConversion framework. The following script reads in molecular information (a SMI file) from a string, adds hydrogens, and writes out an MDL file as a string.

import openbabel

obConversion = openbabel.OBConversion()
obConversion.SetInAndOutFormats("smi", "mdl")
 
mol = openbabel.OBMol()
obConversion.ReadString(mol, "C1=CC=CS1")

print 'Should print 5 (atoms)'
print mol.NumAtoms()

mol.AddHydrogens()
print 'Should print 9 (atoms) after adding hydrogens'
print mol.NumAtoms()

outMDL = obConversion.WriteString(mol)

The following script writes out a file using a filename, rather than reading and writing to a Python string.

import openbabel

obConversion = openbabel.OBConversion()
obConversion.SetInAndOutFormats("pdb", "mol2")

mol = openbabel.OBMol()
obConversion.ReadFile(mol, "1ABC.pdb.gz")   # Open Babel will uncompress automatically

mol.AddHydrogens()

print mol.NumAtoms()
print mol.NumBonds()
print mol.NumResidues()

obConversion.WriteFile(mol, '1abc.mol2')

That's it! There's more information on particular calls in the library API. Feel free to address questions to the openbabel-scripting mailing list.

Using iterators

A number of Open Babel toolkit classes provide iterators over various objects; these classes are identifiable by the suffix "Iter" in the list of toolkit classes in the API. The OBMolAtomIter class, for example, makes it easy to iterate over the atoms in a molecule. These iterator classes can be used using the typical Python syntax for iterators:

for atom in openbabel.OBMolAtomIter(mymol):
    print atom.GetAtomicMass()

Calling a method requiring an array of C doubles

Some Open Babel toolkit methods, for example OBMol::Rotate(), require an array of doubles. It's not possible to directly use a list of floats when calling such a function from Python. Instead, you need to first explicitly create a C array using the double_array() function:

obMol.Rotate([1.0, -54.7, 3])
# Error!
myarray = openbabel.double_array([1.0, -54.7, 3])
obMol.Rotate(myarray)
# Works!

Combining numpy with Open Babel

If you are using the Python numerical extension, numpy, and you try to pass values from a numpy array to Open Babel, it may not work unless you convert the values to Python built-in types first:

import numpy, openbabel
mol = openbabel.OBMol()
atom = mol.NewAtom()

coord = numpy.array([1.2, 2.3, 4.6], "float32")
atom.SetVector(coord[0], coord[1], coord[2])
# Error

atom.SetVector(float(coord[0]), float(coord[1]), float(coord[2]))
# No error

coord = numpy.array([1.2, 2.3, 4.6], "float64")
atom.SetVector(coord[0], coord[1], coord[2])
# No error either - not all numpy arrays will cause an error

Pybel

Pybel provides convenience functions and classes that make it simpler to use the Open Babel libraries from Python, especially for file input/output and for accessing the attributes of atoms and molecules. The Atom and Molecule classes used by Pybel can be converted to and from the OBAtom and OBMol used by the openbabel module. These features are discussed in more detail below.

Information on the Pybel API can be found at the interactive Python prompt using the help() function, and is also available here: Pybel API.

To use Pybel, use "import pybel" or "from pybel import *".

Atoms and Molecules

A Molecule can be created in any of four ways:

1. From an OBMol, using Molecule(myOBMol)
2. By reading from a file (see Input/Output below)
3. By reading from a string (see Input/Output below)
4. An empty Molecule can be created using Molecule()

An Atom can be created in three different ways:

1. From an OBAtom, using Atom(myOBAtom)
2. By accessing the .atoms attribute of a Molecule
3. An empty Atom can be created using Atom()

It is always possible to access the OBMol or OBAtom on which a Molecule or Atom is based, by accessing the appropriate attribute, either .OBMol or .OBAtom. In this way, it is easy to combine the convenience of pybel with the many additional capabilities present in openbabel. See Combining Pybel with openbabel.py below.

Molecules have the following attributes: atoms, charge, data, dim, energy, exactmass, flags, formula, mod, molwt, spin, sssr, title and unitcell (if crystal data). The .atoms attribute provides a list of the Atoms in a Molecule. The .data attribute returns a dictionary of the data fields associated with the molecule, and can be accessed and edited like a normal dictionary. The .unitcell attribute gives access to any unit cell data associated with the molecule (see OBUnitCell). The remaining attributes correspond directly to attributes of OBMols: e.g. Molecule.formula is equivalent to OBMol.GetFormula(). For more information on what these attributes are, please see the Open Babel Library documentation for OBMol.

Molecules have a .write() method that writes a representation of a Molecule to a file or to a string. See Input/Output below. They also have a .calcfp() method that calculates a molecular fingerprint. See Fingerprints below.

For convenience, a Molecule provides an iterator over its Atoms. This is used as follows:

for atom in myMolecule:
   # do something with atom

Atoms have the following attributes: atomicmass, atomicnum, cidx, coords, coordidx, exactmass, formatcharge, heavyvalence, heterovalence, hyb, idx, implicitvalence, index, isotope, partialcharge, spin, type, valence, vector. The .coords attribute provides a tuple (x, y, z) of the atom's coordinates. The remaining attributes are as for OBAtom, and more information can be found in the Open Babel Library documentation.

Input/Output

One of the strengths of Open Babel is the number of chemical file formats that it can handle. Pybel provides a dictionary of the input and output formats in the variables informats and outformats, where the keys are the three-letter codes for each format (e.g. 'pdb') and the values are the descriptions (e.g. 'Protein Data Bank format').

Pybel greatly simplifies the process of reading and writing molecules to and from strings or files. There are two functions for reading Molecules:

1. readstring(format, string) reads a Molecule from a string
2. readfile(format, filename) provides an iterator over the Molecules in a file

Here are some examples of their use. Note in particular the use of .next() to access the first (and possibly only) molecule in a file:

>>> mymol = readstring("smi", "CCCC")
>>> print mymol.molwt
45
>>> for mymol in readfile("sdf", "largeSDfile.sdf")
...	print mymol.molwt
>>> singlemol = readfile("pdb", "1CRN.pdb").next()

If a single molecule is to be written to a molecule or string, the .write() method of the Molecule should be used:

1. mymol.write(format) returns a string
2. mymol.write(format, filename) writes the Molecule to a file. An optional additional parameter, overwrite, should be set to True if you wish to overwrite an existing file.

For files containing multiple molecules, the Outputfile class should be used instead. This is initialised with a format and filename (and optional overwrite parameter). To write a Molecule to the file, the .write() method of the Outputfile is called with the Molecule as a parameter. When all molecules have been written, the .close() method of the Outputfile should be called.

Here are some examples of output using the Pybel methods and classes:

>>> print mymol.write("smi")
'CCCC'
>>> mymol.write("smi", "outputfile.txt")
>>> largeSDfile = Outputfile("sdf", "multipleSD.sdf")
>>> largeSDfile.write(mymol)
>>> largeSDfile.write(myothermol)
>>> largeSDfile.close()

Fingerprints

A Fingerprint can be created in either of two ways:

1. From a vector returned by the OpenBabel GetFingerprint() method, using Fingerprint(myvector)
2. By calling the .calcfp() method of a Molecule

The .calcfp() method takes an optional argument, fptype, which should be one of the fingerprint types supported by OpenBabel (see Tutorial:Fingerprints). If unspecified, the default fingerprint ("FP2") is calculated.

Once created, the Fingerprint has two attributes: fp gives the original OpenBabel vector corresponding to the fingerprint, and bits gives a list of the bits that are set.

The Tanimoto coefficient of two Fingerprints can be calculated using the "|" operator.

Here is an example of its use:

>>> import pybel
>>> smiles = ['CCCC', 'CCCN']
>>> mols = [pybel.readstring("smi", x) for x in smiles] # Create two molecules from the SMILES
>>> fps = [x.calcfp() for x in mols] # Calculate their fingerprints
>>> print fps[0].bits, fps[1].bits
[261, 385, 671] [83, 261, 349, 671, 907]
>>> print fps[0] | fps[1] # Print the Tanimoto coefficient
0.3333

SMARTS matching

Pybel also provides a simplified API to the Open Babel SMARTS pattern matcher. A Smarts object is created, and the .findall() method is then used to return a list of the matches to a given Molecule.

Here is an example of its use:

>>> mol = readstring("smi","CCN(CC)CC") # triethylamine
>>> smarts = Smarts("[#6][#6]") # Matches an ethyl group
>>> print smarts.findall(mol) 
[(1, 2), (4, 5), (6, 7)]

Combining Pybel with openbabel.py

It is easy to combine the ease of use of Pybel, with the comprehensive coverage of the Open Babel toolkit that openbabel.py provides. Pybel is really a wrapper around openbabel.py, with the result that the OBAtom and OBMol used by openbabel.py can be interconverted to the Atom and Molecule used by Pybel.

The following example shows how to read a molecule from a PDB file using Pybel, and then how to use openbabel.py to add hydrogens. It also illustrates how to find out information on what methods and classes are available, while at the interactive Python prompt.

>>> import pybel
>>> mol = pybel.readfile("pdb", "1PYB").next()
>>> help(mol)
Help on Molecule in module pybel object:
...
 |  Attributes:
 |     atoms, charge, dim, energy, exactmass, flags, formula,
 |     mod, molwt, spin, sssr, title.
...
 |  The original Open Babel molecule can be accessed using the attribute:
 |     OBMol
...
>>> print len(mol.atoms), mol.molwt
3430 49315.2
>>> dir(mol.OBMol) # Show the list of methods provided by openbabel.py
['AddAtom', 'AddBond', 'AddConformer', 'AddHydrogens', 'AddPolarHydrogens', ... ]
>>> mol.OBMol.AddHydrogens()
>>> print len(mol.atoms), mol.molwt
7244 49406.0

The next example is an extension of one of the openbabel.py examples at the top of this page. It shows how a molecule could be created using openbabel.py, and then written to a file using Pybel:

import openbabel, pybel

mol = openbabel.OBMol()
a = mol.NewAtom()
a.SetAtomicNum(6)   # carbon atom
a.SetVector(0.0, 1.0, 2.0) # coordinates
b = mol.NewAtom()
mol.AddBond(1, 2, 1)   # atoms indexed from 1

pybelmol = pybel.Molecule(mol)
pybelmol.write("sdf", "outputfile.sdf")