Insilico Structural and Functional Analysis of Covid-19 Genomic Sequences

Clicks: 1
ID: 313117
2024
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal

Ranked #588 of 705 articles by views in Journal of Computing & Biomedical Informatics

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 705 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
The Covid-19 outbreak classified as a pandemic by World Health Organization, is caused by the severe acute respiratory (SARS-CoV-2) syndrome coronavirus 2. The surface glycoprotein or spike (S) protein is one of the four primary structural proteins that SARS-CoV-2 encodes, and it has generally been the focus of research for potential novel vaccines. A number of bioinformatics methods were used in the suggested in silico study to examine the mutational, physicochemical, phylogenetic, structural, and immunological characteristics of spike protein. 81 SARS-CoV-2 sequences from different regions of Pakistan were retrieved from the NCBI database. From all retrieved sequences, the sequences of spike protein were screened out for further analysis. blastp suit available on NCBI web server was employed to align the sequences with reference sequence to analyze mutations in Spike region. SIFT, MUpro, SNAP2, PolyPhen2, PhD-SNP, and I-Mutant were utilized to predict deleterious mutations. Through ProtParam, physiochemical characteristics were analyzed. MEGA11 was used for the phylogenetic analysis, SOPMA and I-TASSER server employed for the investigation of protein secondary and tertiary 3D structures. The position of B-Cell epitopes was predicted using IEDB ElliPro tool. The result of mutation analysis showed 67 mutations in spike region out of which 51 mutations were predicted to be deleterious and affects proteins’ functional stability. Physiochemical analysis showed that this protein was stable in nature. Structural analysis showed that this protein contains random coil as major structure with stable distribution of alpha helix and beta strands. Model 3 was selected for 3D structure build by I-TASSER and verified by 3 tools. ElliPro predicted 21 candidates for epitopes out of which 6 were predicted as potential epitopes by VaxiJen2.0 and AllerTop v2.0. The proposed study makes it easier to understand spike protein in depth, which will be helpful in future research on the infections of SARS-CoV-2 and the construction of diagnostics, antiviral drugs and treatments.
Reference Key
imported_1777059187_69ebc57393e22 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Abdul Majid Soomro
Journal Journal of Computing & Biomedical Informatics
Year 2024
DOI
DOI not found
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.