In Silico Characterization of Hypothetical Protein AZJ53_10480 in Streptococcus pneumoniae

Background. Streptococcus pneumoniae is a major human pathogen responsible for serious infections such as pneumonia. Despite extensive research, many proteins in S. pneumoniae, including hypothetical proteins, remain uncharacterized, limiting the understanding of the bacterium's pathogenic mechanisms. Methods. This study utilizes in silico tools to characterize the hypothetical protein AZJ53_10480 from S. pneumoniae. Sequence alignment and phylogenetic analysis were conducted using BLASTp and ClustalW, while PSIPRED and I-TASSER predicted the protein’s secondary and tertiary structures. Molecular docking studies were performed with AutoDock Vina to assess potential interactions with the antiviral drug sofosbuvir Results. The in silico analysis revealed that the hypothetical protein AZJ53_10480 shares structural and functional similarities with viral capsid proteins of the hepatitis C virus. The protein was found to have a mixed localization, suggesting potential multifunctionality within the bacterial cell. Molecular docking studies indicated a strong binding affinity between AZJ53_10480 and sofosbuvir, suggesting that this protein could be a potential target for therapeutic intervention. Conclusion. This study highlights structural properties and functional roles of hypothetical protein AZJ53_10480 in S. pneumoniae of . The findings suggest that AZJ53_10480 may play a role in the pathogenicity of this bacterium and could serve as a novel target for therapeutic development. Further experimental studies are needed to validate these findings and explore the protein's potential as a drug target. Highlights In silico analysis reveals structural similarities between the hypothetical protein AZJ53_10480 and viral capsid proteins. Docking studies suggest AZJ53_10480 as a potential target for antiviral drugs like sofosbuvir. The study provides new insights into the possible pathogenic role of hypothetical proteins in Streptococcus pneumoniae.

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Publication Details

Journal
BioScientific Review
Published
2024-09-23
DOI
https://doi.org/10.32350/bsr.64.01
Citations
12
Primary Topic
Machine Learning in Bioinformatics
Type
article
Field-Weighted Citation Impact
2.81
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article

In Silico Characterization of Hypothetical Protein AZJ53_10480 in Streptococcus pneumoniae

Sehrish Arshad, Rahmat Ali Khan, Ali Nadeem, Muhammad Asim et al.
12 citations
BioScientific Review
Machine Learning in Bioinformatics
2.81
article

In Silico Characterization of Hypothetical Protein AZJ53_10480 in Streptococcus pneumoniae

Sehrish Arshad, Rahmat Ali Khan, Ali Nadeem, Muhammad Asim, Nimra Hanif, Tanzeel Ur Rehman, Aqsa, Nimra Shafique, Moeez Manzor
article en
12 citations

Abstract

Background. Streptococcus pneumoniae is a major human pathogen responsible for serious infections such as pneumonia. Despite extensive research, many proteins in S. pneumoniae, including hypothetical proteins, remain uncharacterized, limiting the understanding of the bacterium's pathogenic mechanisms. Methods. This study utilizes in silico tools to characterize the hypothetical protein AZJ53_10480 from S. pneumoniae. Sequence alignment and phylogenetic analysis were conducted using BLASTp and ClustalW, while PSIPRED and I-TASSER predicted the protein’s secondary and tertiary structures. Molecular docking studies were performed with AutoDock Vina to assess potential interactions with the antiviral drug sofosbuvir Results. The in silico analysis revealed that the hypothetical protein AZJ53_10480 shares structural and functional similarities with viral capsid proteins of the hepatitis C virus. The protein was found to have a mixed localization, suggesting potential multifunctionality within the bacterial cell. Molecular docking studies indicated a strong binding affinity between AZJ53_10480 and sofosbuvir, suggesting that this protein could be a potential target for therapeutic intervention. Conclusion. This study highlights structural properties and functional roles of hypothetical protein AZJ53_10480 in S. pneumoniae of . The findings suggest that AZJ53_10480 may play a role in the pathogenicity of this bacterium and could serve as a novel target for therapeutic development. Further experimental studies are needed to validate these findings and explore the protein's potential as a drug target. Highlights In silico analysis reveals structural similarities between the hypothetical protein AZJ53_10480 and viral capsid proteins. Docking studies suggest AZJ53_10480 as a potential target for antiviral drugs like sofosbuvir. The study provides new insights into the possible pathogenic role of hypothetical proteins in Streptococcus pneumoniae.

BioScientific ReviewVol. 6(4)
University of Central Punjab (PK), Riphah International University (PK)
Openalex Percentile: Top 9%
Machine Learning in Bioinformatics
2.81
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