PepXPro: a framework for curating, generating, and optimizing structure-affinity protein-peptide datasets
TL;DR
P PepXPro is presented, a modular framework that transforms publicly available protein-peptide structure-affinity resources into curated datasets and reproducible benchmark collections generated under user-defined criteria that provides an extensible foundation for reproducible protein- peptide benchmark construction.
Abstract
Protein-peptide interactions are central to cellular signaling and to a growing class of peptide therapeutics, yet the datasets used to develop and benchmark computational methods for protein-peptide modeling remain poorly standardized. Available databases prioritize comprehensive coverage but require task-specific curation, while published benchmarks are typically distributed as static collections built with heterogeneous curation, quality-filtering, redundancy-reduction, and sampling strategies, limiting reproducibility and cross-study comparison. We present PepXPro, a modular framework that transforms publicly available protein-peptide structure-affinity resources into curated datasets and reproducible benchmark collections generated under user-defined criteria. PepXPro is organized into three components: Scrape, for deterministic curation of protein-peptide complex entries from public resources; GenSample, for constructing configurable subsets under explicit quality, redundancy, and sampling constraints; and Benchmark, for evaluating candidate subsets and selecting a nonredundant, representative, general-purpose benchmark for distribution. Starting from PDBbind and complementary resources, the curation pipeline yields a pool of proteinpeptide complex entries that retains chemically complex cases, including disulfide- linked cyclic peptides, which are commonly excluded from existing benchmarks. We release PepXPro Benchmark v1, a benchmark comprising 70 non-redundant protein- peptide complexes with experimentally determined structures and binding affinities. The underlying framework provides an extensible foundation for reproducible protein- peptide benchmark construction.