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The preservation of the active site architecture, notably the cysteine residue at position 36 (Cys 36 ), coupled with the marked reduction in enzymatic activity exhibited by the GpoA Cys36Ala variant relative to the wild-type enzyme, provides compelling biochemical support for the essential role of this residue in mediating GpoAs peroxidase function

This will enable the construction of a high-resolution map of the molecular landscape, the identification of subtype-specific regulatory nodes and switches (151), and address the fundamental knowledge gaps highlighted in preceding sections, thereby laying a foundation for precise therapeutic targeting