I describe how experimental studies of protein folding have led to advances in protein structure prediction and protein design. I describe the finding that protein sequences are not optimized for rapid folding, the contact order–protein folding rate correlation, the incorporation of experimental insights into protein folding into the Rosetta protein structure production methodology and the use of this methodology to determine structures from sparse experimental data. I then describe the inverse problem (protein design) and give an overview of recent work on designing proteins with new structures and functions. I also describe the contributions of the general public to these efforts through the Rosetta@home distributed computing project and the FoldIt interactive protein folding and design game.
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Conference Article|
March 20 2014
Protein folding, structure prediction and design
David Baker
David Baker
1
*Department of Biochemistry, University of Washington/HMMI, Seattle, WA 98195, U.S.A.
1emaildabaker@uw.edu
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Publisher: Portland Press Ltd
Received:
February 12 2014
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© The Authors Journal compilation © 2014 Biochemical Society
2014
Biochem Soc Trans (2014) 42 (2): 225–229.
Article history
Received:
February 12 2014
Citation
David Baker; Protein folding, structure prediction and design. Biochem Soc Trans 1 April 2014; 42 (2): 225–229. doi: https://doi.org/10.1042/BST20130055
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