A computational framework for exploring structural protein variability in virus variants using a codon network model
DOI:
https://doi.org/10.55630/j.biomath.2025.06.105Keywords:
virus variants, codon network, connected domination, community, centralityAbstract
This study applies a graph-theoretic framework to analyze the structural dynamics of codon networks derived from SARS-CoV-2 spike protein sequences. By employing a dual-level analysis of Minimum Connected Dominating Sets (MCDS) and community structures, we explore the mathematical underpinnings of viral protein organization. First, we construct the MCDS to identify critical codons that ensure global network connectivity, providing key insights into structurally significant regions of the protein sequence. Next, we analyze the community structures within the network to determine localized structural and functional roles, facilitating the identification of specialized codon groups. Centrality measures are employed to quantify the significance of codons within both the MCDS and the identified communities, highlighting their roles in maintaining network integrity. Furthermore, we investigate the impact of mutations across SARS-CoV-2 variants, assessing their influence on codon connectivity and functional stability. A statistical analysis of MCDS and community node variability provides deeper insights into the structural robustness of the spike protein. This study underscores the potential of mathematical modeling in virology and highlights essential codons as potential targets for therapeutic intervention.
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Copyright (c) 2025 L. Praveenkumar, G. Mahadevan, A. A. Navish

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