Simple Ligand–Receptor Interaction Descriptor (SILIRID) for alignment-free binding site comparison

• DOI: 10.1016/j.csbj.2014.05.004
• Publication Date: 2014-06-18T21:59:44Z
• Authors: Vladimir Chupakhin; Gilles Marcou; Helena Gaspar; Alexandre Varnek
• Keywords: 0301 basic medicine; Protein similarity; Article; Protein classification; Generative Topographic Mapping; 03 medical and health sciences; Chemogenomics; [CHIM.CHEM] Chemical Sciences/Cheminformatics; Interaction fingerprints; [CHIM.CHEM]Chemical Sciences/Cheminformatics; TP248.13-248.65; Biotechnology; Protein–ligand interactions

We describe SILIRID (Simple Ligand-Receptor Interaction Descriptor), a novel fixed size descriptor characterizing protein-ligand interactions. SILIRID can be obtained from the binary interaction fingerprints (IFPs) by summing up the bits corresponding to identical amino acids. This results in a vector of 168 integer numbers corresponding to the product of the number of entries (20 amino acids and one cofactor) and 8 interaction types per amino acid (hydrophobic, aromatic face to face, aromatic edge to face, H-bond donated by the protein, H-bond donated by the ligand, ionic bond with protein cation and protein anion, and interaction with metal ion). Efficiency of SILIRID to distinguish different protein binding sites has been examined in similarity search in sc-PDB database, a druggable portion of the Protein Data Bank, using various protein-ligand complexes as queries. The performance of retrieval of structurally and evolutionary related classes of proteins was comparable to that of state-of-the-art approaches (ROC AUC ≈ 0.91). SILIRID can efficiently be used to visualize chemogenomic space covered by sc-PDB using Generative Topographic Mapping (GTM): sc-PDB SILIRID data form clusters corresponding to different protein types.