Literature DB >> 15102452

Theory of protein folding.

José Nelson Onuchic1, Peter G Wolynes.   

Abstract

Protein folding should be complex. Proteins organize themselves into specific three-dimensional structures, through a myriad of conformational changes. The classical view of protein folding describes this process as a nearly sequential series of discrete intermediates. In contrast, the energy landscape theory of folding considers folding as the progressive organization of an ensemble of partially folded structures through which the protein passes on its way to the natively folded structure. As a result of evolution, proteins have a rugged funnel-like landscape biased toward the native structure. Connecting theory and simulations of minimalist models with experiments has completely revolutionized our understanding of the underlying mechanisms that control protein folding.

Mesh:

Year:  2004        PMID: 15102452     DOI: 10.1016/j.sbi.2004.01.009

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


  384 in total

1.  Phi-value analysis and the nature of protein-folding transition states.

Authors:  Alan R Fersht; Satoshi Sato
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-18       Impact factor: 11.205

2.  Relationship of Leffler (Bronsted) alpha values and protein folding Phi values to position of transition-state structures on reaction coordinates.

Authors:  Alan R Fersht
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-21       Impact factor: 11.205

3.  Ultrafast hydration dynamics in protein unfolding: human serum albumin.

Authors:  J K Amisha Kamal; Liang Zhao; Ahmed H Zewail
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-07       Impact factor: 11.205

4.  Hidden complexity of free energy surfaces for peptide (protein) folding.

Authors:  Sergei V Krivov; Martin Karplus
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-04       Impact factor: 11.205

5.  Dynamical transition and proteinquake in photoactive yellow protein.

Authors:  Kazuhito Itoh; Masaki Sasai
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-04       Impact factor: 11.205

6.  Knot formation in newly translated proteins is spontaneous and accelerated by chaperonins.

Authors:  Anna L Mallam; Sophie E Jackson
Journal:  Nat Chem Biol       Date:  2011-12-18       Impact factor: 15.040

Review 7.  Knot theory in understanding proteins.

Authors:  Rama Mishra; Shantha Bhushan
Journal:  J Math Biol       Date:  2011-11-22       Impact factor: 2.259

8.  Dominant folding pathways of a WW domain.

Authors:  Silvio A Beccara; Tatjana Škrbić; Roberto Covino; Pietro Faccioli
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-26       Impact factor: 11.205

9.  Optimizing ring assembly reveals the strength of weak interactions.

Authors:  Eric J Deeds; John A Bachman; Walter Fontana
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-30       Impact factor: 11.205

10.  Cellular reprogramming dynamics follow a simple 1D reaction coordinate.

Authors:  Sai Teja Pusuluri; Alex H Lang; Pankaj Mehta; Horacio E Castillo
Journal:  Phys Biol       Date:  2017-12-06       Impact factor: 2.583

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