Metadata-Version: 2.1
Name: rdkit_utilities
Version: 0.1.0
Summary: UNKNOWN
Home-page: UNKNOWN
Author: Lily Wang
Author-email: lily.wang@anu.edu.au
License: MIT
Platform: Linux
Platform: Mac OS-X
Platform: Unix
Platform: Windows
Requires-Python: >=3.7
Description-Content-Type: text/markdown
License-File: LICENSE

rdkit_utilities
==============================
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Contained here are some helpful RDKit utilities for:

* generating conformers
    * ranking by MMFF electrostatic energy (for ELF conformer selection)
    * selecting to maximise diversity via RMS (for ELF conformer selection)
* finding symmetric atoms in a molecule
* finding the shell of neighbors around a central fragment, N bonds away


There are also convenience functions for:

* loading molecules from any input `MolFromInput`
* loading molecules from SMILES with keyword arguments for `removeHs`, etc.
* loading molecules and reordering by atom map number, analogous to the OpenFF toolkit `Molecule.from_mapped_smiles`
* generally reordering conformers
* optimizing molecules by specifying force field using a string name


Functions are in files such as `rdchem`, `rdDistGeom`, etc. to try to keep to
RDKit's organisation convention. Similarly to RDKit, a `Chem` and `AllChem`
are provided with group imports.
Functions are written in PascalCase and keyword arguments in camelCase, also to
keep to RDKit convention.
### Copyright

Copyright (c) 2022, Lily Wang


#### Acknowledgements
 
Project based on the 
[Computational Molecular Science Python Cookiecutter](https://github.com/molssi/cookiecutter-cms) version 1.5.


