The impact of curation errors in the PDBBind Database on machine learning predictions of protein–protein binding affinity

The PDBBind database has been widely utilized for the computational prediction of protein-protein binding affinities. While the accuracy of the PDBBind-curated equilibrium dissociation constants (KD) has been reported for the protein-ligand subset of the PDBBind database, the curation accuracy has not been reported for the protein-protein subset. Here, we present a detailed manual analysis for the subset of PDBBind records with PubMed Central Open Access primary publications and find that ~19% of these records had KD values that were not supported by their primary publications. The impact of these putative curation errors on the machine learning-based prediction of KD from experimental protein-protein 3D structures was evaluated and correcting the curation errors improved the Pearson correlation coefficient between measured and random forest-predicted log10(KD) values by ~8 percentage points. This finding underscores the importance of dataset accuracy for computational modelling and highlights the need for more stringent curation processes when extracting information from the scientific literature.

Authors

Institutions

Publication Details

Journal
Database
Published
2025-01-01
DOI
https://doi.org/10.1093/database/baaf061
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The impact of curation errors in the PDBBind Database on machine learning predictions of protein–protein binding affinity

Jason Gans, Joshua H. Miller, Nileena Velappan, Esen Sokullu et al.
Database
Protein Structure and Dynamics
article

The impact of curation errors in the PDBBind Database on machine learning predictions of protein–protein binding affinity

Jason Gans, Joshua H. Miller, Nileena Velappan, Esen Sokullu, Ramesh K. Jha
article en

Abstract

The PDBBind database has been widely utilized for the computational prediction of protein-protein binding affinities. While the accuracy of the PDBBind-curated equilibrium dissociation constants (KD) has been reported for the protein-ligand subset of the PDBBind database, the curation accuracy has not been reported for the protein-protein subset. Here, we present a detailed manual analysis for the subset of PDBBind records with PubMed Central Open Access primary publications and find that ~19% of these records had KD values that were not supported by their primary publications. The impact of these putative curation errors on the machine learning-based prediction of KD from experimental protein-protein 3D structures was evaluated and correcting the curation errors improved the Pearson correlation coefficient between measured and random forest-predicted log10(KD) values by ~8 percentage points. This finding underscores the importance of dataset accuracy for computational modelling and highlights the need for more stringent curation processes when extracting information from the scientific literature.

DatabaseVol. 2025
Los Alamos National Laboratory (US)
U.S. Department of Defense, Los Alamos National Laboratory
Openalex Percentile: Top 77%
Protein Structure and Dynamics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.