PubMed · 15093835
Simulating protein evolution in sequence and structure space.
Abstract
Naturally occurring proteins comprise a special subset of all plausible sequences and structures selected through evolution. Simulating protein evolution with simplified and all-atom models has shed light on the evolutionary dynamics of protein populations, the nature of evolved sequences and structures, and the extent to which today's proteins are shaped by selection pressures on folding, structure and function. Extensive mapping of the native structure, stability and folding rate in sequence space using lattice proteins has revealed organizational principles of the sequence/structure map important for evolutionary dynamics. Evolutionary simulations with lattice proteins have highlighted the importance of fitness landscapes, evolutionary mechanisms, population dynamics and sequence space entropy in shaping the generic properties of proteins. Finally, evolutionary-like simulations with all-atom models, in particular computational protein design, have helped identify the dominant selection pressures on naturally occurring protein sequences and structures.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Yu Xia, Michael Levitt. 2004. Simulating protein evolution in sequence and structure space.. https://doi.org/10.1016/j.sbi.2004.03.001
Cite the original work for its findings. Save a collection to share your selection of sources.