Evidence map›Paper›PMID 42390120›Full record

ArticleBioinformatics (Oxford, England)2026

3DICE: interpretable 3D cross-modal learning for drug-target interaction prediction and large-scale drug discovery.

Austin Zi Rui Liu, Nguyen Quoc Khanh Le, Matthew Chin Heng Chua

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Austin Zi Rui LiuRaffles Institution, Singapore, 575954, Singapore.ORCID 0009-0007-9910-6698
Nguyen Quoc Khanh LeAIBioMed Lab, Taipei Medical University, Taipei, 110, Taiwan.ORCID 0000-0003-4896-7926
Matthew Chin Heng ChuaDepartment of Biomedical Informatics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 119615, Singapore.

Funding

National Science and Technology Council NSTC114-2221-E-038-015National Science and Technology Council NSTC115-2221-E-038-012-MY3
6 · The paper itself

Abstract

motivationDrug-target interaction (DTI) prediction is a crucial step in modern drug discovery. Accurate and efficient predictions can substantially reduce costs and development time. Applications of deep learning methods for this purpose have been extensively studied in recent years, yielding instrumental contributions to this field. However, existing methods face issues pertaining to efficient learning of drug and target feature representations, which is detrimental to generalizability and performance in cold-start scenarios. Most approaches extract representations from SMILES strings for drugs and FASTA sequences for target proteins, which encode limited 3D structural information. Additionally, many models lack explainability, being black boxes that provide little physical insight into the underlying mechanisms behind such interactions.

resultsWe propose 3DICE, a novel framework leveraging co-attention-based fusion and massively pre-trained 3D structural encoders for both drugs and proteins. Uni-Mol and ESM-IF1 are employed to generate high-fidelity, 3D structure-aware embeddings which enable richer geometric and chemical understanding. Cross-modal fusion modules further augment representations to model intermolecular binding relationships. Importantly, this mechanism also provides intrinsic interpretability, highlighting and enabling qualitative analysis of most influential atoms or residues. Experiments conducted on two canonical benchmark datasets display the competitiveness of our model in real-world scenarios. 3DICE outperformed state-of-the-art models across multiple metrics on the DrugBank and KIBA datasets. Additional experiments provide a more rigorous analysis of interpretability than is typically reported in prior DTI studies, and we find that attention consistently highlights decision-critical regions which is not intrinsically class-specific. AVAILABILITY: Our model and dataset are freely available at: https://github.com/austinatose/3DICE.

Indexed as

Computational BiologyDeep LearningDrug DiscoveryProteinsSoftwarePharmaceutical PreparationsPharmaceutical PreparationsProteins

Identifiers

PMID42390120
PMCPMC13384055

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LicenceCC BY
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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.