Evidence map›Paper›PMID 40601265›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

CLAPE: Protein-Ligand Binding Site Prediction via Protein Language Models.

Yufan Liu, Boxue Tian

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Yufan LiuComputer Science Program, Computer, Electrical and Mathematical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.
Boxue TianMOE Key Laboratory of Bioinformatics, State Key Laboratory of Molecular Oncology, School of Pharmaceutical Sciences, Tsinghua University, Beijing, China. boxuetian@tsinghua.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-ligand interactions are fundamental to critical biological processes such as transcription, translation, and drug-target interaction. The precise identification of protein-ligand binding residues is essential for accurately modeling these interactions and facilitating subsequent research. However, the development of computational methods that are both efficient and accurate for this purpose remains a significant challenge. Progress in this field holds the potential to drive substantial advancements in biotechnology and drug discovery. In response to this need, we have recently developed a method known as Contrastive Learning And Pretrained Encoder (CLAPE). This approach integrates a pretrained protein language model with contrastive learning to predict ligand-binding residues. In this chapter, we provided a detailed overview of the CLAPE framework, including instructions for using the associated Python package and command-line tools. Additionally, we outline the methods employed for result visualization and describe the comprehensive processes involved in model training.

Indexed as

Computational BiologyProteinsSoftwareBinding SitesHumansLigandsMachine LearningModels, MolecularProtein BindingLigandsProteinsContrastive learningProtein language modelProtein–ligand interaction

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.