Evidence map›Paper›PMID 42912900›Full record

ArticleJournal of chemical information and modeling2026

STELLAR: A Fragment-Based Docking Workflow for Highly Flexible Long-Chain Biopolymers.

Alejandro Rodríguez-Martínez, Jochem Nelen, Miguel Carmena-Bargueño, Carlos Martínez-Cortés, Horacio Pérez-Sánchez

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Alejandro Rodríguez-MartínezStructural Bioinformatics and High Performance Computing Research Group (BIO-HPC), UCAM Universidad Católica de Murcia (UCAM), 30107Murcia, Spain.ORCID 0000-0002-1251-8072
Jochem NelenStructural Bioinformatics and High Performance Computing Research Group (BIO-HPC), UCAM Universidad Católica de Murcia (UCAM), 30107Murcia, Spain.ORCID 0000-0002-9970-4950
Miguel Carmena-BargueñoStructural Bioinformatics and High Performance Computing Research Group (BIO-HPC), UCAM Universidad Católica de Murcia (UCAM), 30107Murcia, Spain.ORCID 0000-0002-2735-4859
Carlos Martínez-CortésStructural Bioinformatics and High Performance Computing Research Group (BIO-HPC), UCAM Universidad Católica de Murcia (UCAM), 30107Murcia, Spain.ORCID 0000-0002-5029-3089
Horacio Pérez-SánchezStructural Bioinformatics and High Performance Computing Research Group (BIO-HPC), UCAM Universidad Católica de Murcia (UCAM), 30107Murcia, Spain.ORCID 0000-0003-4468-7898

Funding

Comunidad Aut?noma de la Regi?n de Murcia NAFundaci?n Cient?fica Asociaci?n Espa?ola Contra el C?ncer PRDMU246084RODRFundaci?n S?neca 22616/PI/24NextGenerationEU PRTR-C17.I1Rupicapra Investigaciones, A.I.E. NA
6 · The paper itself

Abstract

Docking methods have improved significantly through optimization using generative approaches and systematic exploration of parameter configurations within docking software. However, docking large molecules such as peptides remains challenging, while the docking of large non-peptidic biopolymers is still insufficiently explored. Existing tools often exhibit limitations in both accuracy and computational efficiency when applied to longer peptides or other polymers. Moreover, although generative deep learning and machine learning approaches have shown promise, they still frequently lack robust ranking metrics, resulting in suboptimal performance. To address these limitations, we developed STELLAR (Score-Tuning for Efficient Ranking of Large Ligands using an Accurate and Refined Docking Configuration), a workflow designed to enable efficient and accurate docking of highly flexible long-chain biopolymers exceeding 10 subunits. STELLAR implements a fragment-based strategy, decomposing the biopolymer into smaller units for individual docking, followed by recomposition into full-length structures. It also includes optimized algorithms for handling long-chain biopolymers. The pipeline integrates structural optimization steps using tools such as GNINA, RDKit, and GROMACS, ensuring physically realistic poses. STELLAR achieved RMSD values below 5 Å in validation experiments using benchmark complexes from Propedia and the Protein Data Bank (PDB). It offers a faster and more efficient alternative to several state-of-the-art tools across a range of peptide lengths. Additionally, it scales linearly in computational time, runs primarily on CPUs with minimal GPU usage, avoids reliance on generative approximations, provides an accurate metric for ligand ranking, and reduces computational cost compared to similar tools. Its design also supports high-throughput screening of linear polymer-protein interactions by efficiently reducing the complexity associated with high conformational flexibility.

Indexed as

Molecular Docking SimulationAlgorithmsBiopolymersLigandsProtein ConformationProteinsSoftwareWorkflowBiopolymersLigandsProteins

Identifiers

PMID42912900
PMCPMC13663479

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.