Literature DB >> 10986128

A rapid test for identification of autonomous folding units in proteins.

K F Fischer1, S Marqusee.   

Abstract

The structure of a protein is dictated by a large number of weak interactions that cooperatively stabilize the native state. Usually, excised fragments smaller than a domain have little if any residual structure. When autonomous units of structure are found within domains, this challenges common assumptions about the cooperativity of protein structure. Such autonomous folding units (AFUs) are of wide interest and have applications in protein engineering and as simple model systems for studying the determinants of stability and specificity. A new method of identifying AFUs within proteins is presented here. The rapid autonomous fragment test (RAFT) identifies AFUs based on analysis of inter-residue contacts present in the three-dimensional structure of a protein. RAFT is fast enough to mine the entire PDB for AFUs and provide a library of potential small stable folds. We show that RAFT is able to predict whether a protein fragment will be structured if isolated from its parent domain. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10986128     DOI: 10.1006/jmbi.2000.4049

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  16 in total

1.  Contributions of folding cores to the thermostabilities of two ribonucleases H.

Authors:  Srebrenka Robic; James M Berger; Susan Marqusee
Journal:  Protein Sci       Date:  2002-02       Impact factor: 6.725

2.  Experimental evaluation of topological parameters determining protein-folding rates.

Authors:  Erik J Miller; Kael F Fischer; Susan Marqusee
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

3.  Dynamic protein domains: identification, interdependence, and stability.

Authors:  Semen O Yesylevskyy; Valery N Kharkyanen; Alexander P Demchenko
Journal:  Biophys J       Date:  2006-04-21       Impact factor: 4.033

4.  Exploring subdomain cooperativity in T4 lysozyme I: structural and energetic studies of a circular permutant and protein fragment.

Authors:  Jason Cellitti; Manuel Llinas; Nathaniel Echols; Elizabeth A Shank; Blake Gillespie; Ester Kwon; Scott M Crowder; Frederick W Dahlquist; Tom Alber; Susan Marqusee
Journal:  Protein Sci       Date:  2007-03-30       Impact factor: 6.725

5.  Branching in the sequential folding pathway of cytochrome c.

Authors:  Mallela M G Krishna; Haripada Maity; Jon N Rumbley; S Walter Englander
Journal:  Protein Sci       Date:  2007-07-27       Impact factor: 6.725

Review 6.  Protein folding and misfolding: mechanism and principles.

Authors:  S Walter Englander; Leland Mayne; Mallela M G Krishna
Journal:  Q Rev Biophys       Date:  2008-04-14       Impact factor: 5.318

7.  Modulating long-range energetics via helix stabilization: A case study using T4 lysozyme.

Authors:  Sabriya N Rosemond; Kambiz M Hamadani; Jamie H D Cate; Susan Marqusee
Journal:  Protein Sci       Date:  2018-12       Impact factor: 6.725

8.  Evidence for close side-chain packing in an early protein folding intermediate previously assumed to be a molten globule.

Authors:  Laura E Rosen; Katelyn B Connell; Susan Marqusee
Journal:  Proc Natl Acad Sci U S A       Date:  2014-09-25       Impact factor: 11.205

9.  Detecting hidden sequence propensity for amyloid fibril formation.

Authors:  Sukjoon Yoon; William J Welsh
Journal:  Protein Sci       Date:  2004-08       Impact factor: 6.725

10.  SPROUTS: a database for the evaluation of protein stability upon point mutation.

Authors:  Mathieu Lonquety; Zoé Lacroix; Nikolaos Papandreou; Jacques Chomilier
Journal:  Nucleic Acids Res       Date:  2008-10-22       Impact factor: 16.971

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