Literature DB >> 17124867

A structure-centric view of protein evolution, design, and adaptation.

Eric J Deeds1, Eugene I Shakhnovich.   

Abstract

Proteins, by virtue of their central role in most biological processes, represent one of the key subjects of the study of molecular evolution. Inherent in the indispensability of proteins for living cells is the fact that a given protein can adopt a specific three-dimensional shape that is specified solely by the protein's sequence of amino acids. Over the past several decades, structural biologists have demonstrated that the array of structures that proteins may adopt is quite astounding, and this has lead to a strong interest in understanding how protein structures change and evolve over time. In this review we consider a large body of recent work that attempts to illuminate this structure-centric picture of protein evolution. Much of this work has focused on the question of how completely new protein structures (i.e., new folds or topologies) are discovered by protein sequences as they evolve. Pursuant to this question of structural innovation has been a desire to describe and understand the observation that certain types of protein structures are far more abundant than others and how this uneven distribution of proteins implicates on the process through which new shapes are discovered. We consider a number of theoretical models that have been successful at explaining this heterogeneity in protein populations and discuss the increasing amount of evidence that indicates that the process of structural evolution involves the divergence of protein sequences and structures from one another. We also consider the topic of protein designability, which concerns itself with understanding how a protein's structure influences the number of sequences that can fold successfully into that structure. Understanding and quantifying the relationship between the physical feature of a structure and its designability has been a long-standing goal of the study of protein structure and evolution, and we discuss a number of recent advances that have yielded a promising answer to this question. Finally, we review the relatively new field of protein structural phylogeny, an area of study in which information about the distribution of protein structures among different organisms is used to reconstruct the evolutionary relationships between them. Taken together, the work that we review presents an increasingly coherent picture of how these unique polymers have evolved over the course of life on Earth.

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Year:  2007        PMID: 17124867     DOI: 10.1002/9780471224464.ch2

Source DB:  PubMed          Journal:  Adv Enzymol Relat Areas Mol Biol        ISSN: 0065-258X


  11 in total

1.  Intra-chain 3D segment swapping spawns the evolution of new multidomain protein architectures.

Authors:  András Szilágyi; Yang Zhang; Péter Závodszky
Journal:  J Mol Biol       Date:  2011-11-04       Impact factor: 5.469

2.  Artificial domain duplication replicates evolutionary history of ketol-acid reductoisomerases.

Authors:  Jackson K B Cahn; Sabine Brinkmann-Chen; Andrew R Buller; Frances H Arnold
Journal:  Protein Sci       Date:  2015-12-21       Impact factor: 6.725

3.  The subtle benefits of being promiscuous: adaptive evolution potentiated by enzyme promiscuity.

Authors:  Mark A Depristo
Journal:  HFSP J       Date:  2007-07-10

4.  Detecting evolutionary relationships across existing fold space, using sequence order-independent profile-profile alignments.

Authors:  Lei Xie; Philip E Bourne
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-02       Impact factor: 11.205

5.  Robust protein protein interactions in crowded cellular environments.

Authors:  Eric J Deeds; Orr Ashenberg; Jaline Gerardin; Eugene I Shakhnovich
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-11       Impact factor: 11.205

Review 6.  Merging molecular mechanism and evolution: theory and computation at the interface of biophysics and evolutionary population genetics.

Authors:  Adrian W R Serohijos; Eugene I Shakhnovich
Journal:  Curr Opin Struct Biol       Date:  2014-06-19       Impact factor: 6.809

7.  Evolutionary divergence of duplicate copies of the growth hormone gene in suckers (Actinopterygii: catostomidae).

Authors:  Henry L Bart; Paulette C Reneau; Michael H Doosey; Charles D Bell
Journal:  Int J Mol Sci       Date:  2010-03-16       Impact factor: 5.923

8.  ProteomeVis: a web app for exploration of protein properties from structure to sequence evolution across organisms' proteomes.

Authors:  Rostam M Razban; Amy I Gilson; Niamh Durfee; Hendrik Strobelt; Kasper Dinkla; Jeong-Mo Choi; Hanspeter Pfister; Eugene I Shakhnovich
Journal:  Bioinformatics       Date:  2018-10-15       Impact factor: 6.937

9.  Universal features in the genome-level evolution of protein domains.

Authors:  Marco Cosentino Lagomarsino; Alessandro L Sellerio; Philip D Heijning; Bruno Bassetti
Journal:  Genome Biol       Date:  2009-01-30       Impact factor: 13.583

10.  Stylus: a system for evolutionary experimentation based on a protein/proteome model with non-arbitrary functional constraints.

Authors:  Douglas D Axe; Brendan W Dixon; Philip Lu
Journal:  PLoS One       Date:  2008-06-04       Impact factor: 3.240

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