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The term "multiple bacterial enzymes and proteins" encompasses a very broad group of bacterial macromolecules serving catalytic, structural, or regulatory functions in pathogenic and commensal bacteria. These molecules include specific enzymes (such as proteases, kinases, and transferases), structural proteins, transporters, and regulatory proteins that together sustain bacterial survival, virulence, and resistance mechanisms[1][4][7][8]. Many of these proteins are key therapeutic targets in antibacterial drug development, as their inhibition can cripple essential bacterial pathways, protein synthesis, cell wall biogenesis, or resistance processes. Due to the extensive diversity in bacterial protein families, modern drug discovery uses computational and genome-scale approaches to identify, classify, and prioritize these targets for novel therapy[1][7][10]. However, the non-specific group label cannot be mapped to a single drug target or biomarker and should be replaced by the explicit names of individual bacterial proteins or enzyme targets for downstream structured data analysis[3][5].
Enzyme inhibition (blocking essential bacterial enzymes); Covalent modification (irreversible inhibition, e.g., β-lactam antibiotics); Disruption of cell wall biosynthesis; Interference with protein synthesis; Inhibition of virulence factor activity; Inhibition of resistance mechanisms
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