Stereo Perception Performed by Open Babel

This section provides a quick introduction on the stereo perception performed by Open Babel, which is the process of constructing stereo centers with stereoinformation received from input data.

What Is the Stereo Perception performed by Open Babel? - Stereo perception performed by Open Babel is the process of constructing stereo centers with stereoinformation received from input data.

Stereo perception is performed in the following order of precedence:

1. Constructing stereo centers with 3D stereoinformation from input data. A symmetry analysis identifies stereogenic centers whose stereo-configurations are perceived from the coordinates.

2. Adding stereo centers with 2D stereoinformation from input data. This is done based on a symmetry analysis, and their configuration inferred either from the geometry (for cis/trans bonds) or from bonds marked as wedge/hash (tetrahedral centers). Only new stereo centers are added. Existing stereo centers perceived from 3D stereoinformation are not changed.

3. Adding stereo centers with 0D stereoinformation from input data depends on the format of input data. Here are two examples:

Note that, if both 3D and 2D stereoinformation are provided for the same stereo center, 3D stereoinformation wins.

Table of Contents

 About This Book

 SMILES (Simplified Molecular-Input Line-Entry System)

 Open Babel: The Open Source Chemistry Toolbox

 Using Open Babel Command: "obabel"

 Generating SVG Pictures with Open Babel

 Substructure Search with Open Babel

 Similarity Search with Open Babel

 Fingerprint Index for Fastsearch with Open Babel

Stereochemistry with Open Babel

 What Is Stereochemistry

 Read Stereoinformation from Input with Open Babel

Stereo Perception Performed by Open Babel

 Write Stereoinformation to Output by Open Babel

 Wedge-Hash Bond Changed by Open Babel

 Hash Bond with Solid Line by Open Babel

 Hash over Double Bond by Open Babel

 Command Line Tools Provided by Open Babel

 RDKit: Open-Source Cheminformatics Software

 rdkit.Chem.rdchem - The Core Module

 rdkit.Chem.rdmolfiles - Molecular File Module

 rdkit.Chem.rdDepictor - Compute 2D Coordinates

 rdkit.Chem.Draw - Handle Molecule Images

 Molecule Substructure Search with RDKit

 rdkit.Chem.rdmolops - Molecule Operations

 Daylight Fingerprint Generator in RDKit

 Morgan Fingerprint Generator in RDKit

 RDKit Performance on Substructure Search

 Introduction to Molecular Fingerprints

 OCSR (Optical Chemical Structure Recognition)

 AlphaFold - Protein Structure Prediction

 Resources and Tools

 Cheminformatics Related Terminologies

 References

 Full Version in PDF/EPUB