Literature DB >> 11101895

An evolutionary bridge to a new protein fold.

M H Cordes1, R E Burton, N P Walsh, C J McKnight, R T Sauer.   

Abstract

Arc repressor bearing the N11L substitution (Arc-N11L) is an evolutionary intermediate between the wild type protein, in which the region surrounding position 11 forms a beta-sheet, and a double mutant 'switch Arc', in which this region is helical. Here, Arc-N11L is shown to be able to adopt either the wild type or mutant conformations. Exchange between these structures occurs on the millisecond time scale in a dynamic equilibrium in which the relative populations of each fold depend on temperature, solvent conditions and ligand binding. The N11L mutation serves as an evolutionary bridge from the beta-sheet to the helical fold because in the mutant, Leu is an integral part of the hydrophobic core of the new structure but can also occupy a surface position in the wild type structure. Conversely, the polar Asn 11 side chain serves as a negative design element in wild type Arc because it cannot be incorporated into the core of the mutant fold.

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Year:  2000        PMID: 11101895     DOI: 10.1038/81985

Source DB:  PubMed          Journal:  Nat Struct Biol        ISSN: 1072-8368


  29 in total

1.  Recombinatoric exploration of novel folded structures: a heteropolymer-based model of protein evolutionary landscapes.

Authors:  Yan Cui; Wing Hung Wong; Erich Bornberg-Bauer; Hue Sun Chan
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

2.  Retroevolution of lambda Cro toward a stable monomer.

Authors:  Kelly R LeFevre; Matthew H J Cordes
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-21       Impact factor: 11.205

3.  On hydrophobicity and conformational specificity in proteins.

Authors:  Erik Sandelin
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

4.  Metamorphic proteins mediate evolutionary transitions of structure.

Authors:  Itamar Yadid; Noam Kirshenbaum; Michal Sharon; Orly Dym; Dan S Tawfik
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-05       Impact factor: 11.205

5.  Examination of the quality of various force fields and solvation models for the equilibrium simulations of GA88 and GB88.

Authors:  Juan Zeng; Yongxiu Li; John Z H Zhang; Ye Mei
Journal:  J Mol Model       Date:  2016-07-08       Impact factor: 1.810

6.  Sequence determinants of a conformational switch in a protein structure.

Authors:  Thomas A Anderson; Matthew H J Cordes; Robert T Sauer
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-12       Impact factor: 11.205

7.  A folding space odyssey.

Authors:  Alan R Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-19       Impact factor: 11.205

8.  A structural model of latent evolutionary potentials underlying neutral networks in proteins.

Authors:  Richard Wroe; Hue Sun Chan; Erich Bornberg-Bauer
Journal:  HFSP J       Date:  2007-05-21

9.  Mutagenic dissection of the sequence determinants of protein folding, recognition, and machine function.

Authors:  Robert T Sauer
Journal:  Protein Sci       Date:  2013-09-18       Impact factor: 6.725

10.  Evolutionary bridges to new protein folds: design of C-terminal Cro protein chameleon sequences.

Authors:  William J Anderson; Laura O Van Dorn; Wendy M Ingram; Matthew H J Cordes
Journal:  Protein Eng Des Sel       Date:  2011-06-14       Impact factor: 1.650

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