Literature DB >> 10211821

Factors limiting the performance of prediction-based fold recognition methods.

X de la Cruz1, J M Thornton.   

Abstract

In the past few years, a new generation of fold recognition methods has been developed, in which the classical sequence information is combined with information obtained from secondary structure and, sometimes, accessibility predictions. The results are promising, indicating that this approach may compete with potential-based methods (Rost B et al., 1997, J Mol Biol 270:471-480). Here we present a systematic study of the different factors contributing to the performance of these methods, in particular when applied to the problem of fold recognition of remote homologues. Our results indicate that secondary structure and accessibility prediction methods have reached an accuracy level where they are not the major factor limiting the accuracy of fold recognition. The pattern degeneracy problem is confirmed as the major source of error of these methods. On the basis of these results, we study three different options to overcome these limitations: normalization schemes, mapping of the coil state into the different zones of the Ramachandran plot, and post-threading graphical analysis.

Mesh:

Year:  1999        PMID: 10211821      PMCID: PMC2144320          DOI: 10.1110/ps.8.4.750

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


  37 in total

1.  Protein fold recognition using sequence-derived predictions.

Authors:  D Fischer; D Eisenberg
Journal:  Protein Sci       Date:  1996-05       Impact factor: 6.725

2.  The structural alignment between two proteins: is there a unique answer?

Authors:  A Godzik
Journal:  Protein Sci       Date:  1996-07       Impact factor: 6.725

3.  Sequences annotated by structure: a tool to facilitate the use of structural information in sequence analysis.

Authors:  D Milburn; R A Laskowski; J M Thornton
Journal:  Protein Eng       Date:  1998-10

4.  Protein fold recognition by mapping predicted secondary structures.

Authors:  R B Russell; R R Copley; G J Barton
Journal:  J Mol Biol       Date:  1996-06-14       Impact factor: 5.469

5.  Evaluation of threading specificity and accuracy.

Authors:  S H Bryant
Journal:  Proteins       Date:  1996-10

6.  The new genomics: global views of biology.

Authors:  E S Lander
Journal:  Science       Date:  1996-10-25       Impact factor: 47.728

7.  Protein fold recognition by threading: comparison of algorithms and analysis of results.

Authors:  D R Westhead; V P Collura; M D Eldridge; M A Firth; J Li; C W Murray
Journal:  Protein Eng       Date:  1995-12

8.  Protein structure prediction by threading methods: evaluation of current techniques.

Authors:  C M Lemer; M J Rooman; S J Wodak
Journal:  Proteins       Date:  1995-11

9.  Confronting the problem of interconnected structural changes in the comparative modeling of proteins.

Authors:  R Samudrala; J T Pedersen; H B Zhou; R Luo; K Fidelis; J Moult
Journal:  Proteins       Date:  1995-11

10.  Intrinsic phi, psi propensities of amino acids, derived from the coil regions of known structures.

Authors:  M B Swindells; M W MacArthur; J M Thornton
Journal:  Nat Struct Biol       Date:  1995-07
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  3 in total

1.  Toward predicting protein topology: an approach to identifying beta hairpins.

Authors:  Xavier de la Cruz; E Gail Hutchinson; Adrian Shepherd; Janet M Thornton
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-12       Impact factor: 11.205

2.  Prediction of the beta-hairpins in proteins using support vector machine.

Authors:  Xiu Zhen Hu; Qian Zhong Li
Journal:  Protein J       Date:  2008-02       Impact factor: 2.371

Review 3.  From local structure to a global framework: recognition of protein folds.

Authors:  Agnel Praveen Joseph; Alexandre G de Brevern
Journal:  J R Soc Interface       Date:  2014-04-16       Impact factor: 4.118

  3 in total

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