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Proteases emerging from the first round of dual selection, including X(PC3)a and X(PC3)c, showed decreased activity on VAMP1 (Extended Data Fig

To understand how NK1 activates c-MET, we determined the cryo-EM structure of the 2:2 c-MET/NK1 complex at an overall 5 resolution (Supplementary Figs

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These early findings open pathways for future investigation into how fat metabolism peptides might intersect with cardiovascular disease models