Literature DB >> 27288744

The thermostability and specificity of ancient proteins.

Lucas C Wheeler1, Shion A Lim2, Susan Marqusee3, Michael J Harms4.   

Abstract

Were ancient proteins systematically different than modern proteins? The answer to this question is profoundly important, shaping how we understand the origins of protein biochemical, biophysical, and functional properties. Ancestral sequence reconstruction (ASR), a phylogenetic approach to infer the sequences of ancestral proteins, may reveal such trends. We discuss two proposed trends: a transition from higher to lower thermostability and a tendency for proteins to acquire higher specificity over time. We review the evidence for elevated ancestral thermostability and discuss its possible origins in a changing environmental temperature and/or reconstruction bias. We also conclude that there is, as yet, insufficient data to support a trend from promiscuity to specificity. Finally, we propose future work to understand these proposed evolutionary trends.
Copyright © 2016. Published by Elsevier Ltd.

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Year:  2016        PMID: 27288744      PMCID: PMC5010474          DOI: 10.1016/j.sbi.2016.05.015

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  53 in total

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  37 in total

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4.  Evolutionary trend toward kinetic stability in the folding trajectory of RNases H.

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6.  FireProtASR: A Web Server for Fully Automated Ancestral Sequence Reconstruction.

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8.  The burst-phase folding intermediate of ribonuclease H changes conformation over evolutionary history.

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9.  Conservation of Specificity in Two Low-Specificity Proteins.

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