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The role of dynamic conformational ensembles in biomolecular recognition

aureus resolves this dilemma by employing CstB, a persulfide dioxygenase-rhodanese fusion (PRF), that we show is promiscuous towards persulfide substrates

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TB-500 Cellular Mechanisms and Receptor Interactions Actin-Binding Domain Functionality TB-500 functions primarily through high-affinity interactions with G-actin monomers, preventing spontaneous polymerisation and maintaining cytoplasmic actin pools in monomeric form