| Literature DB >> 30555007 |
Catherine R Knoverek1, Gaya K Amarasinghe2, Gregory R Bowman3.
Abstract
A protein is a dynamic shape-shifter whose function is determined by the set of structures it adopts. Unfortunately, atomically detailed structures are only available for a few conformations of any given protein, and these structures have limited explanatory and predictive power. Here, we provide a brief historical perspective on protein dynamics and introduce recent advances in computational and experimental methods that are providing unprecedented access to protein shape-shifting. Next, we focus on how these tools are revealing the mechanism of allosteric communication and features like cryptic pockets; both of which present new therapeutic opportunities. A major theme is the importance of considering the relative probabilities of different structures and the control one can exert over protein function by modulating this balance.Entities:
Keywords: allostery; cryptic pockets; protein dynamics
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Year: 2018 PMID: 30555007 PMCID: PMC6422738 DOI: 10.1016/j.tibs.2018.11.007
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807