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Interestingly, SMAX1 D2 co-precipitated more MAX2 when SMAX1 N was added in trans, indicating that binding of the two domains is cooperative, possibly through stabilising MAX2

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In addition, a biodistribution study revealed greater accumulation of PF-PTX in tumor sites than did free drugs [204]

The substrate engages the complex through two domains, forming a dynamic interface that stabilises the receptorligase assembly and repositions the ASK1, suggesting a mechanism for efficient ubiquitination