This interaction is highly significant, as Gln385 is known to be a pivotal residue, experimentally validated to stabilize the natural substrate cyclodityrosine and other CYP121 inhibitors.
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Efficient synthesis, dual anti-tubercular and antioxidant activity of triazole-acetophenone derivatives: enhanced efficacy <i>via</i> esterification and quantum mechanical validation of CYP121 binding.
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