FUSED: A Functional Representation for Joint Structural and Elemental Analysis of Protein Ligand Binding Sites
- 1Texas Tech University
Abstract
Ligand binding site representations are central to the analysis of protein-ligand interactions, with applications in functional characterization, binding-site comparison, and ligand recognition. Many descriptor-based approaches characterize ligand binding sites using a fixed distance threshold from the ligand, despite substantial variability in how such thresholds are defined and the possibility that relevant structural and compositional information changes across spatial scales. We propose Functional Unification of Structural and Elemental Descriptors (FUSED), a multivariate functional representation that jointly models structural and elemental compositional information of ligand binding sites as functions of distance from the ligand. Structural information is captured through covariance-based descriptors derived from the CDPA framework, while chemical composition is represented through isometric log-ratio coordinates to account appropriately for compositional geometry. Treating distance from the ligand as a functional domain allows structural and compositional characteristics to be examined across distance thresholds rather than at a single prespecified value. The resulting representation can be used directly or combined with dimension-reduction, statistical-learning, and/or machine-learning procedures, with the distance interval tailored to the dataset, analytical task, and procedure. We evaluate FUSED on three benchmark datasets spanning complementary ligand binding-site analysis tasks: the Extended Kahraman dataset for multiclass ligand discrimination, TOUGH-C1 for binary binding-site classification, and TOUGH-M1 for pairwise matching of pockets associated with drug-like ligands. FUSED supports strong discrimination in the EK and TOUGH-C1 tasks using standard statistical-learning procedures, while a supervised Siamese neural network applied to the full FUSED representation achieves a mean ROC-AUC of 0.9375 on TOUGH-M1 under repeated sequence-cluster-disjoint evaluation, approaching the strongest reported benchmark performance. These results demonstrate that FUSED provides a flexible, alignment-free representation that supports both direct examination of threshold-dependent binding-site characteristics and competitive downstream classification and pocket matching while remaining computationally practical.
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BibTeX
@misc{priyankara2026fused,
title = {{FUSED: A Functional Representation for Joint Structural and Elemental Analysis of Protein Ligand Binding Sites}},
author = {T. M. S. Priyankara and L. Ellingson},
howpublished = {bioRxiv},
year = {2026},
month = jul,
doi = {10.64898/2026.07.10.737806},
url = {https://www.biorxiv.org/content/10.64898/2026.07.10.737806v2},
note = {CC BY},
}
RIS
TY - UNPB
TI - FUSED: A Functional Representation for Joint Structural and Elemental Analysis of Protein Ligand Binding Sites
AU - T. M. S. Priyankara
AU - L. Ellingson
PY - 2026
DA - 2026/07/10
PB - bioRxiv
DO - 10.64898/2026.07.10.737806
UR - https://www.biorxiv.org/content/10.64898/2026.07.10.737806v2
AB - Ligand binding site representations are central to the analysis of protein-ligand interactions, with applications in functional characterization, binding-site comparison, and ligand recognition. Many descriptor-based approaches characterize ligand binding sites using a fixed distance threshold from the ligand, despite substantial variability in how such thresholds are defined and the possibility that relevant structural and compositional information changes across spatial scales. We propose Functional Unification of Structural and Elemental Descriptors (FUSED), a multivariate functional representation that jointly models structural and elemental compositional information of ligand binding sites as functions of distance from the ligand. Structural information is captured through covariance-based descriptors derived from the CDPA framework, while chemical composition is represented through isometric log-ratio coordinates to account appropriately for compositional geometry. Treating distance from the ligand as a functional domain allows structural and compositional characteristics to be examined across distance thresholds rather than at a single prespecified value. The resulting representation can be used directly or combined with dimension-reduction, statistical-learning, and/or machine-learning procedures, with the distance interval tailored to the dataset, analytical task, and procedure. We evaluate FUSED on three benchmark datasets spanning complementary ligand binding-site analysis tasks: the Extended Kahraman dataset for multiclass ligand discrimination, TOUGH-C1 for binary binding-site classification, and TOUGH-M1 for pairwise matching of pockets associated with drug-like ligands. FUSED supports strong discrimination in the EK and TOUGH-C1 tasks using standard statistical-learning procedures, while a supervised Siamese neural network applied to the full FUSED representation achieves a mean ROC-AUC of 0.9375 on TOUGH-M1 under repeated sequence-cluster-disjoint evaluation, approaching the strongest reported benchmark performance. These results demonstrate that FUSED provides a flexible, alignment-free representation that supports both direct examination of threshold-dependent binding-site characteristics and competitive downstream classification and pocket matching while remaining computationally practical.
ER -