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A decoupled alignment kernel for peptide membrane permeability predictions

delete2026-08-04
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OA
AI
A
Ali Amirahmadi *
G
Gökçe Geylan
L
Leonardo De Maria
F
Farzaneh Etminani
M
Mattias Ohlsson
A
Alessandro Tibo
DOI:10.1186/s13321-026-01276-5delete
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Abstract

Abstract

En 中文
Cyclic peptides are promising modalities for targeting intracellular sites; however, cell-membrane permeability remains a key bottleneck, exacerbated by limited public data and the need for well-calibrated uncertainty. Instead of relying on data-eager complex deep learning architecture, we propose a monomer-aware decoupled global alignment kernel (MD-GAK), which couples chemically meaningful residue–residue similarity with sequence alignment while decoupling local matches from gap penalties. MD-GAK is a relatively simple kernel. To further demonstrate the robustness of our framework, we also introduce a variant, PMD-GAK, which incorporates a triangular positional prior. As we will show in the experimental section, PMD-GAK can offer additional advantages over MD-GAK, particularly in reducing calibration errors. Since our focus is on uncertainty estimation, we use Gaussian Processes as the predictive model, as both MD-GAK and PMD-GAK can be directly applied within this framework. We demonstrate the effectiveness of our methods through an extensive set of experiments, comparing our fully reproducible approach against state-of-the-art models, and show that it outperforms them across all metrics. Scientific contribution We introduce monomer-aware decoupled global alignment kernels for Gaussian processes (MD-GAK and position-aware PMD-GAK) that align cyclic peptides at the sequence level using chemically rich monomer fingerprints and explicit positional priors, yielding positive-definite similarity measures tailored to permeability modeling. Compared with order-agnostic fingerprint methods, standard global-alignment kernels and state-of-the-art graph and language-model baselines, our alignment-aware GPs provide improved discrimination, probabilistic calibration and scaffold-level robustness under stringent, leakage-controlled cyclic-peptide permeability benchmarks.
Keywords:
Cyclic peptides
Permeability
Gaussian processes
Global alignment kernel
Tanimoto
Calibration

Journal

Journal of Cheminformatics cover
Journal of Cheminformatics
IF:
5.7
Papers:
1.4K
Citations:
1.1W

Organization

D
Department of Life Sciences
Scholars:
611
Papers: 279
Citations: 6
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