Literature DB >> 11327757

Evolutionary conservation of the folding nucleus.

L Mirny1, E Shakhnovich.   

Abstract

Here, we present statistical analysis of conservation profiles in families of homologous sequences for nine proteins whose folding nucleus was determined by protein engineering methods. We show that in all but one protein (AcP) folding nucleus residues are significantly more conserved than the rest of the protein. Two aspects of our study are especially important: (i) grouping of amino acid residues into classes according to their physical-chemical properties and (ii) proper normalization of amino acid probabilities that reflects the fact that evolutionary pressure to conserve some amino acid types may itself affect concentration of various amino acid types in protein families. Neglect of any of those two factors may make physical and biological "signals" from conservation profiles disappear. Copyright 2001 Academic Press.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11327757     DOI: 10.1006/jmbi.2001.4602

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


  46 in total

1.  Persistently conserved positions in structurally similar, sequence dissimilar proteins: roles in preserving protein fold and function.

Authors:  Iddo Friedberg; Hanah Margalit
Journal:  Protein Sci       Date:  2002-02       Impact factor: 6.725

2.  ArchDB: automated protein loop classification as a tool for structural genomics.

Authors:  Jordi Espadaler; Narcis Fernandez-Fuentes; Antonio Hermoso; Enrique Querol; Francesc X Aviles; Michael J E Sternberg; Baldomero Oliva
Journal:  Nucleic Acids Res       Date:  2004-01-01       Impact factor: 16.971

3.  Coarse-grained sequences for protein folding and design.

Authors:  Scott Brown; Nicolas J Fawzi; Teresa Head-Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-08       Impact factor: 11.205

4.  NMR structure of the forkhead-associated domain from the Arabidopsis receptor kinase-associated protein phosphatase.

Authors:  Gui-In Lee; Zhaofeng Ding; John C Walker; Steven R Van Doren
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-18       Impact factor: 11.205

5.  Simulation, experiment, and evolution: understanding nucleation in protein S6 folding.

Authors:  Isaac A Hubner; Mikael Oliveberg; Eugene I Shakhnovich
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-18       Impact factor: 11.205

6.  Thermodynamic stability explains the differential evolutionary dynamics of cytochrome b and COX I in mammals.

Authors:  Juan Carlos Aledo; Héctor Valverde; Manuel Ruíz-Camacho
Journal:  J Mol Evol       Date:  2012-02-24       Impact factor: 2.395

7.  Protein subunit interfaces: A statistical analysis of hot spots in Sm proteins.

Authors:  Srđan D Stojanović; Božidarka L Zarić; Snežana D Zarić
Journal:  J Mol Model       Date:  2010-07-23       Impact factor: 1.810

8.  Fold and flexibility: what can proteins' mechanical properties tell us about their folding nucleus?

Authors:  Sophie Sacquin-Mora
Journal:  J R Soc Interface       Date:  2015-11-06       Impact factor: 4.118

9.  Evolution of a protein folding nucleus.

Authors:  Xue Xia; Liam M Longo; Mason A Sutherland; Michael Blaber
Journal:  Protein Sci       Date:  2015-12-10       Impact factor: 6.725

10.  Automatic generation and evaluation of sparse protein signatures for families of protein structural domains.

Authors:  Matthew J Blades; Jon C Ison; Ranjeeva Ranasinghe; John B C Findlay
Journal:  Protein Sci       Date:  2005-01       Impact factor: 6.725

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.