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However, due to the required experimental conditions of fragment screening by XRD (where crystals are exposed to fragment molecules at very high concentrations – tens to hundreds of millimolar) there is an increased chance of observing “false positive” binding sites
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in the 1940s, GUS has emerged as a pivotal enzymatic mediator of glucuronide deconjugation, thereby counteracting glucuronidation through deconjugation of glucuronide metabolites [17]
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