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Swan, J. A.

Publications and source records attributed to Swan, J. A..

2 recordsLinked to original sources

Mechanistic classification of the AAA superfamily with protein language models

The ATPases Associated with various cellular Activites (AAA) are a class of proteins with diverse structure-function relationships whereby conserved 3-dimensional architecture is employed in varied mechanistic contexts. While cryo-electron microscopy has revealed extensive mechanistic data, predicting how specific sequence elements dictate unique biochemical mechanisms remains a challenge. Here, we present a machine learning framework to resolve these sequence-function relationships. We established a hierarchical classification scheme based on five distinct modes of coupling ATP hydrolysis to mechanical work. Using CatFunc, a lightweight protein language model (PLM)-based pipeline, we leveraged evolutionary context from millions of protein sequences for supervised classification of AAA domains based on mechanism. We observed excellent recall of our mechanistic annotations in masked validation studies, demonstrating that domain level context is sufficient to encapsulate the various observed mechanisms. Notably, systematic misclassifications revealed a shared evolutionary and mechanistic ancestry within the rotary motor class. Applying the model to out-of-distribution proteomic datasets, we established metrics to detect unrepresented functions. Our framework provides a scalable strategy for decoding molecular function from sequence data, offering a transferable approach for other biomedically important families such as membrane transporters, G protein-coupled receptors and kinases.

biochemistry↗

Structural mimicry confers robustness in the cyanobacterial circadian clock

The histidine kinase SasA enhances robustness of circadian rhythms in the cyanobacterium S. elongatus by temporally controlling expression of the core clock components, kaiB and kaiC. Here we show that SasA also engages directly with KaiB and KaiC proteins to regulate the period and enhance robustness of the reconstituted circadian oscillator in vitro, particularly under limiting concentrations of KaiB. In contrast to its role regulating gene expression, oscillator function does not require SasA kinase activity; rather, SasA uses structural mimicry to cooperatively recruit the rare, fold-switched conformation of KaiB to the KaiC hexamer to form the nighttime repressive complex. Cooperativity gives way to competition with increasing concentrations of SasA to define a dynamic window by which SasA directly modulates clock robustness. One Sentence SummarySasA controls the assembly of clock protein complexes through a balance of cooperative and competitive interactions.

biochemistry↗