Literature DB >> 16379537

The victor/FRST function for model quality estimation.

Silvio C E Tosatto1.   

Abstract

Scoring functions are widely used in the final step of model selection in protein structure prediction. This is of interest both for comparative modeling targets, where it is important to select the best model among a set of many good, "correct" ones, as well as for other (fold recognition or novel fold) targets, where the set may contain many incorrect models. A novel combination of four knowledge-based potentials recognizing different features of native protein structures is introduced and tested. The pairwise, solvation, hydrogen bond, and torsion angle potentials contain largely orthogonal information. Of these, the torsion angle potential is found to show the strongest correlation with model quality. Combining these features with a linear weighting function, it was possible to construct a robust energy function capable of discriminating native-like structures on several benchmarking sets. In a recent blind test (CAFASP-4 MQAP), the scoring function ranked consistently well and was able to reliably distinguish the correct template from an ensemble of high quality decoys in 52 of 70 cases (33 of 34 for comparative modeling). An executable version of the Victor/FRST function for Linux PCs is available for download from the URL http://protein.cribi.unipd.it/frst/.

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Year:  2005        PMID: 16379537     DOI: 10.1089/cmb.2005.12.1316

Source DB:  PubMed          Journal:  J Comput Biol        ISSN: 1066-5277            Impact factor:   1.479


  42 in total

1.  A composite score for predicting errors in protein structure models.

Authors:  David Eramian; Min-yi Shen; Damien Devos; Francisco Melo; Andrej Sali; Marc A Marti-Renom
Journal:  Protein Sci       Date:  2006-06-02       Impact factor: 6.725

2.  Local quality assessment in homology models using statistical potentials and support vector machines.

Authors:  Marc Fasnacht; Jiang Zhu; Barry Honig
Journal:  Protein Sci       Date:  2007-06-28       Impact factor: 6.725

3.  The war of tools: how can NMR spectroscopists detect errors in their structures?

Authors:  Edoardo Saccenti; Antonio Rosato
Journal:  J Biomol NMR       Date:  2008-03-05       Impact factor: 2.835

4.  IRECS: a new algorithm for the selection of most probable ensembles of side-chain conformations in protein models.

Authors:  Christoph Hartmann; Iris Antes; Thomas Lengauer
Journal:  Protein Sci       Date:  2007-06-13       Impact factor: 6.725

Review 5.  Mycoplasma lipoproteins and Toll-like receptors.

Authors:  Ling-ling Zuo; Yi-mou Wu; Xiao-xing You
Journal:  J Zhejiang Univ Sci B       Date:  2009-01       Impact factor: 3.066

6.  Contribution of the distal pocket residue to the acyl-chain-length specificity of (R)-specific enoyl-coenzyme A hydratases from Pseudomonas spp.

Authors:  Takeharu Tsuge; Shun Sato; Ayaka Hiroe; Koya Ishizuka; Hiromi Kanazawa; Yoshitsugu Shiro; Tamao Hisano
Journal:  Appl Environ Microbiol       Date:  2015-09-18       Impact factor: 4.792

7.  QMEAN server for protein model quality estimation.

Authors:  Pascal Benkert; Michael Künzli; Torsten Schwede
Journal:  Nucleic Acids Res       Date:  2009-05-08       Impact factor: 16.971

8.  Improved estimation of structure predictor quality.

Authors:  Kevin W DeRonne; George Karypis
Journal:  BMC Struct Biol       Date:  2009-06-30

9.  A computational model of the LGI1 protein suggests a common binding site for ADAM proteins.

Authors:  Emanuela Leonardi; Simonetta Andreazza; Stefano Vanin; Giorgia Busolin; Carlo Nobile; Silvio C E Tosatto
Journal:  PLoS One       Date:  2011-03-29       Impact factor: 3.240

10.  QMEANclust: estimation of protein model quality by combining a composite scoring function with structural density information.

Authors:  Pascal Benkert; Torsten Schwede; Silvio Ce Tosatto
Journal:  BMC Struct Biol       Date:  2009-05-20
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