John Paul Pezacki, Eryn Lundrigan, Parrish Evers, Spencer Uguccioni
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引用次数: 0
Abstract
Determining the ligandability of the human proteome can provide key insights to characterize biological processes and promote drug discovery. Now, multi-tiered activity-based protein profiling provides comprehensive proteomic maps of chiral small-molecule interactions. Over 300 distinctive proteins were identified to ligand tryptoline acrylamides, including stereoselective and site-specific events.
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