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May 9, 2026Journal of Chemical Theory and Computation4 citationsOpen Access

Predicting and Decoding Allosteric Binding Sites Using Protein Language Models and Structure-Based Machine Learning: An Energy Landscape-Guided Explainable AI Framework

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KRKamila RiedlováVŠVít ŠkrhákWGWilliam G. Gatlin

Key Points

  • This research aims to evaluate how well allosteric binding sites can be predicted in protein structures using advanced computational methods.
  • Used a fine-tuned protein language model alongside the P2Rank structure-based method to analyze 453 human kinases.
  • Employed energy landscape frustration analysis to interpret predictability differences between orthosteric and allosteric sites.
  • Integrated prediction results with local frustration analysis for physical interpretability of binding site organization.
  • High precision in identifying orthosteric ATP-binding sites with low prediction confidence in allosteric sites.
  • Analysis shows that orthosteric pockets are in minimally frustrated energy basins, while allosteric pockets are in neutrally frustrated zones.
  • Identifies local energetic embedding as a significant factor affecting predictive visibility for binding sites.

Abstract

Computational prediction of allosteric binding sites in protein structures remains a persistent challenge, as these regulatory pockets evade detection by both sequence-based and structure-based algorithms. Both computational and physical origins of this predictive asymmetry remain insufficiently understood. In this study, we systematically examine the determinants of binding site predictability using a dual framework that integrates a fine-tuned protein language model and the structure-based method P2Rank as complementary tools probing a diverse data set of 453 human kinases, together with a physics-based interpretability layer derived from energy landscape frustration analysis. Both predictors exhibit a sharp and reproducible dichotomy on protein kinases, in which orthosteric ATP-binding sites can be identified with high precision, whereas allosteric sites are detected with substantially lower confidence across kinase structures and distinct conformational states. To decode this divergence, we deploy energy landscape-based explainable AI approach that integrates local frustration analysis as an independent physical interpretability layer, mapping predictive behavior to the underlying energetic organization of protein structures. This analysis reveals that predictive success is governed by the local energetic embedding of binding sites within the protein energy landscape. Orthosteric pockets are located in minimally frustrated basins that generate strong evolutionary and structural signatures, whereas allosteric pockets occupy predominantly neutrally frustrated zones associated with conformational plasticity and reduced evolutionary constraint. By integrating the prediction results with energy landscape analysis, our framework converts predictive performance into physically interpretable descriptors of binding site organization in protein kinases. These results establish energy landscape frustration as a potentially important determinant of algorithmic visibility and an interpretability layer providing a feasible strategy for diagnosing the limits of current prediction methods.

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Cite This Study

Riedlová et al. (2026) studied this question.

synapsesocial.com/papers/69fed153b9154b0b82878aa4https://doi.org/10.1021/acs.jctc.6c00427
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