Evidence map›Paper›PMID 39844339›Full record

ArticleBriefings in bioinformatics2024

TargetCLP: clathrin proteins prediction combining transformed and evolutionary scale modeling-based multi-view features via weighted feature integration approach.

Matee Ullah, Shahid Akbar, Ali Raza, Kashif Ahmad Khan, Quan Zou

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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.

Matee UllahInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan 610054, China.ORCID 0009-0008-9461-6290
Shahid AkbarInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan 610054, China.ORCID 0000-0002-1106-0012
Ali RazaDepartment of Computer Science, MY University, Islamabad 45750, Pakistan.
Kashif Ahmad KhanDepartment of Computer Science, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
Quan ZouInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan 610054, China.ORCID 0000-0001-6406-1142

Funding

National Natural Science Foundation of China 62450002National Science and Technology Major Project 2022ZD0117700
6 · The paper itself

Abstract

Clathrin proteins, key elements of the vesicle coat, play a crucial role in various cellular processes, including neural function, signal transduction, and endocytosis. Disruptions in clathrin protein functions have been associated with a wide range of diseases, such as Alzheimer's, neurodegeneration, viral infection, and cancer. Therefore, correctly identifying clathrin protein functions is critical to unravel the mechanism of these fatal diseases and designing drug targets. This paper presents a novel computational method, named TargetCLP, to precisely identify clathrin proteins. TargetCLP leverages four single-view feature representation methods, including two transformed feature sets (PSSM-CLBP and RECM-CLBP), one qualitative characteristics feature, and one deep-learned-based embedding using ESM. The single-view features are integrated based on their weights using differential evolution, and the BTG feature selection algorithm is utilized to generate a more optimal and reduced subset. The model is trained using various classifiers, among which the proposed SnBiLSTM achieved remarkable performance. Experimental and comparative results on both training and independent datasets show that the proposed TargetCLP offers significant improvements in terms of both prediction accuracy and generalization to unseen data, furthering advancements in the research field.

Indexed as

ClathrinComputational BiologyEvolution, MolecularSoftwareAlgorithmsDatabases, ProteinHumansClathrinclathrin proteinfeature integrationprotein language model, transformed featuresself-normalized modelsequence analysis

Identifiers

PMID39844339
PMCPMC11753890

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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.