Literature DB >> 12786198

Distances and classification of amino acids for different protein secondary structures.

Xin Liu1, Li-mei Zhang, Shan Guan, Wei-Mou Zheng.   

Abstract

Window profiles of amino acids in protein sequences are used to describe the amino acid environment. The relative entropy or Kullback-Leibler distance derived from these profiles is used as a measure of dissimilarity for comparison of amino acids and secondary structure conformations. Distance matrices of amino acid pairs at different conformations are obtained, which display a non-negligible dependence of amino acid similarity on conformations. Based on the conformation specific distances, a clustering analysis for amino acids is conducted.

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Year:  2003        PMID: 12786198     DOI: 10.1103/PhysRevE.67.051927

Source DB:  PubMed          Journal:  Phys Rev E Stat Nonlin Soft Matter Phys        ISSN: 1539-3755


  5 in total

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Authors:  C Etchebest; C Benros; A Bornot; A-C Camproux; A G de Brevern
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2.  Switch region for pathogenic structural change in conformational disease and its prediction.

Authors:  Xin Liu; Ya-Pu Zhao
Journal:  PLoS One       Date:  2010-01-11       Impact factor: 3.240

3.  Automated alphabet reduction for protein datasets.

Authors:  Jaume Bacardit; Michael Stout; Jonathan D Hirst; Alfonso Valencia; Robert E Smith; Natalio Krasnogor
Journal:  BMC Bioinformatics       Date:  2009-01-06       Impact factor: 3.169

4.  Fast dynamics perturbation analysis for prediction of protein functional sites.

Authors:  Dengming Ming; Judith D Cohn; Michael E Wall
Journal:  BMC Struct Biol       Date:  2008-01-30

5.  Donut-shaped fingerprint in homologous polypeptide relationships--a topological feature related to pathogenic structural changes in conformational disease.

Authors:  Xin Liu; Ya-Pu Zhao
Journal:  J Theor Biol       Date:  2009-02-25       Impact factor: 2.691

  5 in total

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