Evidence map›Paper›PMID 40460206›Full record

ArticleVeterinary medicine and science2025

Structural, Functional and Inhibitory Annotations of Lumpy Skin Disease Virus Hypothetical Protein LSDV004: An In-Silico Study.

F M Yasir Hasib, Md Shafiqul Islam

Abstract read
In one paragraph

Article in Veterinary medicine and science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Review
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4 · The record

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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.

F M Yasir HasibDepartment of Pathology and Parasitology, Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University, Chattogram, Bangladesh.ORCID 0000-0002-6662-7725
Md Shafiqul IslamDepartment of Pathology and Parasitology, Faculty of Veterinary Medicine, Chattogram Veterinary and Animal Sciences University, Chattogram, Bangladesh.ORCID 0000-0003-2248-917X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lumpy skin disease virus (LSDV) is the etiological agent of lumpy skin disease (LSD), predominantly afflicting cattle populations and posing significant economic implications to the livestock industry. Despite the comprehensive genome sequencing of LSDV, several hypothetical genes with unknown functions remain, potentially playing pivotal roles in disease pathogenesis and serving as targets for drug discovery. This study aimed to explore the LSDV004 gene by predicting its key properties, structure, functions and potential inhibitors using bioinformatic tools. Physiochemical analysis using ExPASy ProtParam indicates LSDV004 is a stable protein with an instability index below 40, suggesting structural stability. Secondary structure analysis via SOPMA identifies the random coil as the predominant structural element, covering 50.88% of residues, followed by extended strands (36.84%). The tertiary structure predicted and refined using SWISS-MODEL and GalaxyRefine respectively, > 90% of residues in the favoured region of the Ramachandran plot, according to PROCHECK validation. Functional prediction highlights structural similarities with the Swinepox virus C2 and suggests potential involvement in pathways such as negative regulation of gene expression, as indicated by gene ontology (GO) analysis using I-TASSER. Moreover, the GO analysis indicates functional similarity with anti-apoptotic protein Bcl-2-like protein 1 (PDB ID: 1LXL). Molecular docking studies with HDOCK reveal pelcitoclax as exhibiting better docking characteristics compared to other Bcl-2 inhibitors. However, it's important to note that these predictions require validation through wet laboratory experiments to confirm the LSV004 protein's structural, functional and inhibitory properties. These findings suggest LSDV004's role in LSD pathogenesis and its potential as a drug target and also highlight areas for further experimental studies to confirm its function, supporting efforts toward effective treatments and control.

Indexed as

Lumpy Skin DiseaseLumpy skin disease virusViral ProteinsAnimalsCattleComputer SimulationViral Proteinshypothetical proteinin‐silicoLSDV004lumpy skin diseaselumpy skin disease virus

Identifiers

PMID40460206
PMCPMC12132776

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