Computational Protein Structural Annotations of Mycobacterium tuberculosis Thiamine Phosphate Pyrophosphorylase

Background: (Mtb) is the causative agent of tuberculosis (TB), a respiratory infection characterized by persistent lung infection. The development of drug resistance in Mtb poses a significant challenge in treating TB patients, necessitating the discovery of new therapeutic targets. Materials and Methods: In this study, bioinformatic methods were employed to investigate the structure and function of Mtb-Thiamine phosphate pyrophosphorylase (TPPase) at a molecular level. As an X-ray/nuclear magnetic resonance crystallographic structure was unavailable in the protein databank, a homology protein model of TPPase was created using the X-ray structures of TPPase as templates, following homology modelling method. The resulting Mtb-TPPase protein structure was assessed for quality, including stereochemical prediction using Ramachandran plot, Procheck, and Prosa. Key structural and functional residues of Mtb-TPPase were identified using the crystal structure of TPPase. Results: The homology model of TPPase, constructed using the above-mentioned methods, exhibited a high-quality protein structure that satisfied stereochemical predictions. The model retained the topological and functional properties of the TPPase protein family. The Mtb-TPPase model demonstrated suitability for molecular interactions, such as drug-protein interactions, as indicated by energy and Ramachandran plot values. These findings provide valuable insights for designing TPPase inhibitors and structure-based drug design approaches. Conclusion: The constructed homology model of Mtb-TPPase presents a tertiary structure that can be utilized for designing selective and specific Mtb-TPPase inhibitors. However, further investigations involving computational docking and high-throughput screening experiments are required to gather more detailed information and validate the model's potential applications.