Literature DB >> 8445636

Empirical and structural models for insertions and deletions in the divergent evolution of proteins.

S A Benner1, M A Cohen, G H Gonnet.   

Abstract

The exhaustive matching of the protein sequence database makes possible a broadly based study of insertions and deletions (indels) during divergent evolution. In this study, the probability of a gap in an alignment of a pair of homologous protein sequences was found to increase with the evolutionary distance measured in PAM units (number of accepted point mutations per 100 amino acid residues). A relationship between the average number of amino acid residues between indels and evolutionary distance suggests that a unit 30 to 40 amino acid residues in length remains, on average, undisrupted by indels during divergent evolution. Further, the probability of a gap was found to be inversely proportional to gap length raised to the 1.7 power. This empirical law fits closely over the entire range of gap lengths examined. Gap length distribution is largely independent of evolutionary distance. These results rule out the widely used linear gap penalty as a satisfactory formula for scoring gaps when constructing alignments. Further, the observed gap length distribution can be explained by a simple model of selective pressures governing the acceptance of indels during divergent evolution. Finally, this model provides theoretical support for using indels as part of "parsing algorithms", important in the de novo prediction of the folded structure of proteins from the sequence data.

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Year:  1993        PMID: 8445636     DOI: 10.1006/jmbi.1993.1105

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


  59 in total

1.  Modeling of loops in protein structures.

Authors:  A Fiser; R K Do; A Sali
Journal:  Protein Sci       Date:  2000-09       Impact factor: 6.725

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Journal:  Genome Res       Date:  2002-12       Impact factor: 9.043

3.  Frequency of gaps observed in a structurally aligned protein pair database suggests a simple gap penalty function.

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Journal:  Nucleic Acids Res       Date:  2004-05-20       Impact factor: 16.971

4.  Analysis of protein homology by assessing the (dis)similarity in protein loop regions.

Authors:  Anna R Panchenko; Thomas Madej
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5.  Rapid evolution in conformational space: a study of loop regions in a ubiquitous GTP binding domain.

Authors:  Christian Blouin; Davin Butt; Andrew James Roger
Journal:  Protein Sci       Date:  2004-03       Impact factor: 6.725

6.  Mechanisms of protein oligomerization, the critical role of insertions and deletions in maintaining different oligomeric states.

Authors:  Kosuke Hashimoto; Anna R Panchenko
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-03       Impact factor: 11.205

7.  An information theoretic approach to macromolecular modeling: I. Sequence alignments.

Authors:  Tiba Aynechi; Irwin D Kuntz
Journal:  Biophys J       Date:  2005-11       Impact factor: 4.033

8.  Ngila: global pairwise alignments with logarithmic and affine gap costs.

Authors:  Reed A Cartwright
Journal:  Bioinformatics       Date:  2007-03-25       Impact factor: 6.937

9.  Problems and solutions for estimating indel rates and length distributions.

Authors:  Reed A Cartwright
Journal:  Mol Biol Evol       Date:  2008-11-28       Impact factor: 16.240

10.  Evolution of the genetic code by incorporation of amino acids that improved or changed protein function.

Authors:  Brian R Francis
Journal:  J Mol Evol       Date:  2013-06-07       Impact factor: 2.395

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