AHoJ-DB: A PDB-wide Assignment of apo & holo Relationships Based on Individual Protein-Ligand Interactions

J Mol Biol. 2024 Sep 1;436(17):168545. doi: 10.1016/j.jmb.2024.168545. Epub 2024 Mar 18.

Abstract

A single protein structure is rarely sufficient to capture the conformational variability of a protein. Both bound and unbound (holo and apo) forms of a protein are essential for understanding its geometry and making meaningful comparisons. Nevertheless, docking or drug design studies often still consider only single protein structures in their holo form, which are for the most part rigid. With the recent explosion in the field of structural biology, large, curated datasets are urgently needed. Here, we use a previously developed application (AHoJ) to perform a comprehensive search for apo-holo pairs for 468,293 biologically relevant protein-ligand interactions across 27,983 proteins. In each search, the binding pocket is captured and mapped across existing structures within the same UniProt, and the mapped pockets are annotated as apo or holo, based on the presence or absence of ligands. We assemble the results into a database, AHoJ-DB (www.apoholo.cz/db), that captures the variability of proteins with identical sequences, thereby exposing the agents responsible for the observed differences in geometry. We report several metrics for each annotated pocket, and we also include binding pockets that form at the interface of multiple chains. Analysis of the database shows that about 24% of the binding sites occur at the interface of two or more chains and that less than 50% of the total binding sites processed have an apo form in the PDB. These results can be used to train and evaluate predictors, discover potentially druggable proteins, and reveal protein- and ligand-specific relationships that were previously obscured by intermittent or partial data. Availability: www.apoholo.cz/db.

Keywords: Apo-holo; binding sites; drug design; ligands; protein structure.

MeSH terms

  • Apoproteins / chemistry
  • Apoproteins / metabolism
  • Binding Sites
  • Computational Biology / methods
  • Databases, Protein*
  • Humans
  • Ligands
  • Models, Molecular
  • Protein Binding*
  • Protein Conformation*
  • Proteins* / chemistry
  • Proteins* / metabolism

Substances

  • Ligands
  • Proteins
  • Apoproteins