Literature DB >> 9321415

Estimation of evolutionary distances from protein spatial structures.

N V Grishin1.   

Abstract

New equations are derived to estimate the number of amino acid substitutions per site between two homologous proteins from the root mean square (RMS) deviation between two spatial structures and from the fraction of identical residues between two sequences. The equations are based on evolutionary models, analyzing predominantly structural changes and not sequence changes. Evolution of spatial structure is treated as a diffusion in an elastic force field. Diffusion accounts for structural changes caused by amino acid substitutions, and elastic force reflects selection, which preserves protein fold. Obtained equations are supported by analysis of protein spatial structures.

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Year:  1997        PMID: 9321415     DOI: 10.1007/pl00006241

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  15 in total

1.  Estimation of the number of amino acid substitutions per site when the substitution rate varies among sites.

Authors:  N V Grishin
Journal:  J Mol Evol       Date:  1995-11       Impact factor: 2.395

2.  Comparison of solvent-inaccessible cores of homologous proteins: definitions useful for protein modelling.

Authors:  T J Hubbard; T L Blundell
Journal:  Protein Eng       Date:  1987-06

3.  On the PAM matrix model of protein evolution.

Authors:  W J Wilbur
Journal:  Mol Biol Evol       Date:  1985-09       Impact factor: 16.240

4.  Fitting discrete probability distributions to evolutionary events.

Authors:  T Uzzell; K W Corbin
Journal:  Science       Date:  1971-06-11       Impact factor: 47.728

5.  Property and efficiency of the maximum likelihood method for molecular phylogeny.

Authors:  N Saitou
Journal:  J Mol Evol       Date:  1988       Impact factor: 2.395

6.  Comparison of conformational characteristics in structurally similar protein pairs.

Authors:  T P Flores; C A Orengo; D S Moss; J M Thornton
Journal:  Protein Sci       Date:  1993-11       Impact factor: 6.725

7.  Relative efficiencies of the maximum-likelihood, neighbor-joining, and maximum-parsimony methods when substitution rate varies with site.

Authors:  Y Tateno; N Takezaki; M Nei
Journal:  Mol Biol Evol       Date:  1994-03       Impact factor: 16.240

8.  Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites.

Authors:  Z Yang
Journal:  Mol Biol Evol       Date:  1993-11       Impact factor: 16.240

9.  The spatial distribution of fixed mutations within genes coding for proteins.

Authors:  R Holmquist; M Goodman; T Conroy; J Czelusniak
Journal:  J Mol Evol       Date:  1983       Impact factor: 2.395

10.  The relation between the divergence of sequence and structure in proteins.

Authors:  C Chothia; A M Lesk
Journal:  EMBO J       Date:  1986-04       Impact factor: 11.598

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  14 in total

1.  From complete genomes to measures of substitution rate variability within and between proteins.

Authors:  N V Grishin; Y I Wolf; E V Koonin
Journal:  Genome Res       Date:  2000-07       Impact factor: 9.043

2.  Evolution and topology in the yeast protein interaction network.

Authors:  Stefan Wuchty
Journal:  Genome Res       Date:  2004-07       Impact factor: 9.043

3.  A stochastic evolutionary model for protein structure alignment and phylogeny.

Authors:  Christopher J Challis; Scott C Schmidler
Journal:  Mol Biol Evol       Date:  2012-06-21       Impact factor: 16.240

4.  Divergent evolution within protein superfolds inferred from profile-based phylogenetics.

Authors:  Douglas L Theobald; Deborah S Wuttke
Journal:  J Mol Biol       Date:  2005-09-20       Impact factor: 5.469

5.  Comparison of sequence-based and structure-based phylogenetic trees of homologous proteins: Inferences on protein evolution.

Authors:  S Balaji; N Srinivasan
Journal:  J Biosci       Date:  2007-01       Impact factor: 1.826

6.  BAYESIAN PROTEIN STRUCTURE ALIGNMENT.

Authors:  Abel Rodriguez; Scott C Schmidler
Journal:  Ann Appl Stat       Date:  2014-12-19       Impact factor: 2.083

7.  Simultaneous Bayesian estimation of alignment and phylogeny under a joint model of protein sequence and structure.

Authors:  Joseph L Herman; Christopher J Challis; Ádám Novák; Jotun Hein; Scott C Schmidler
Journal:  Mol Biol Evol       Date:  2014-06-04       Impact factor: 16.240

8.  KH domain: one motif, two folds.

Authors:  N V Grishin
Journal:  Nucleic Acids Res       Date:  2001-02-01       Impact factor: 16.971

9.  The combined effects of amino acid substitutions and indels on the evolution of structure within protein families.

Authors:  Zheng Zhang; Yuxiao Wang; Lushan Wang; Peiji Gao
Journal:  PLoS One       Date:  2010-12-13       Impact factor: 3.240

10.  Comparative Bioinformatic Analysis of Active Site Structures in Evolutionarily Remote Homologues of α,β-Hydrolase Superfamily Enzymes.

Authors:  D A Suplatov; V K Arzhanik; V K Svedas
Journal:  Acta Naturae       Date:  2011-01       Impact factor: 1.845

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