Literature DB >> 22057923

CONTSOR--a new knowledge-based fold recognition potential, based on side chain orientation and contacts between residue terminal groups.

Boris Vishnepolsky1, Malak Pirtskhalava.   

Abstract

Recognizing the structural similarity without significant sequence identity (fold recognition) is an effective method for protein structure prediction. Previously, we developed a fold recognition potential called SORDIS, which incorporated side chain orientation in relation to hydrophobic core centers, distance of the residues from the protein globule center and secondary structure terms. But this potential does not include terms, based on close contacts between residues. In this paper a new fold recognition potential CONTSOR was presented, which based on SORDIS terms and the term, based on contacts between amino acid terminal groups. The performance of this potential was evaluated on SABmark benchmark for alignment accuracy and on SABmark and Lindahl benchmarks for fold recognition. The results show that CONTSOR has the best performance among other potentials on SABmark benchmark both for alignment accuracy and fold recognition and one of the best performances on Lindahl benchmark. CONTSOR software package is available for download at http://www.lifescience.org.ge/downloads/contsor.zip.
Copyright © 2011 The Protein Society.

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Year:  2011        PMID: 22057923      PMCID: PMC3323788          DOI: 10.1002/pro.763

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  64 in total

1.  Amino acid substitution matrices from protein blocks.

Authors:  S Henikoff; J G Henikoff
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

2.  Topology fingerprint approach to the inverse protein folding problem.

Authors:  A Godzik; A Kolinski; J Skolnick
Journal:  J Mol Biol       Date:  1992-09-05       Impact factor: 5.469

3.  Exhaustive matching of the entire protein sequence database.

Authors:  G H Gonnet; M A Cohen; S A Benner
Journal:  Science       Date:  1992-06-05       Impact factor: 47.728

4.  A new approach to protein fold recognition.

Authors:  D T Jones; W R Taylor; J M Thornton
Journal:  Nature       Date:  1992-07-02       Impact factor: 49.962

5.  SCOP: a structural classification of proteins database for the investigation of sequences and structures.

Authors:  A G Murzin; S E Brenner; T Hubbard; C Chothia
Journal:  J Mol Biol       Date:  1995-04-07       Impact factor: 5.469

6.  A structural basis for sequence comparisons. An evaluation of scoring methodologies.

Authors:  M S Johnson; J P Overington
Journal:  J Mol Biol       Date:  1993-10-20       Impact factor: 5.469

7.  A new substitution matrix for protein sequence searches based on contact frequencies in protein structures.

Authors:  S Miyazawa; R L Jernigan
Journal:  Protein Eng       Date:  1993-04

8.  Polar and nonpolar atomic environments in the protein core: implications for folding and binding.

Authors:  P Koehl; M Delarue
Journal:  Proteins       Date:  1994-11

9.  Factors influencing the ability of knowledge-based potentials to identify native sequence-structure matches.

Authors:  J P Kocher; M J Rooman; S J Wodak
Journal:  J Mol Biol       Date:  1994-02-04       Impact factor: 5.469

10.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.

Authors:  J D Thompson; D G Higgins; T J Gibson
Journal:  Nucleic Acids Res       Date:  1994-11-11       Impact factor: 16.971

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  1 in total

1.  Virtual interactomics of proteins from biochemical standpoint.

Authors:  Jaroslav Kubrycht; Karel Sigler; Pavel Souček
Journal:  Mol Biol Int       Date:  2012-08-08
  1 in total

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