Literature DB >> 10191147

GenTHREADER: an efficient and reliable protein fold recognition method for genomic sequences.

D T Jones1.   

Abstract

A new protein fold recognition method is described which is both fast and reliable. The method uses a traditional sequence alignment algorithm to generate alignments which are then evaluated by a method derived from threading techniques. As a final step, each threaded model is evaluated by a neural network in order to produce a single measure of confidence in the proposed prediction. The speed of the method, along with its sensitivity and very low false-positive rate makes it ideal for automatically predicting the structure of all the proteins in a translated bacterial genome (proteome). The method has been applied to the genome of Mycoplasma genitalium, and analysis of the results shows that as many as 46 % of the proteins derived from the predicted protein coding regions have a significant relationship to a protein of known structure. In some cases, however, only one domain of the protein can be predicted, giving a total coverage of 30 % when calculated as a fraction of the number of amino acid residues in the whole proteome. Copyright 1999 Academic Press.

Entities:  

Mesh:

Year:  1999        PMID: 10191147     DOI: 10.1006/jmbi.1999.2583

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


  253 in total

1.  MODBASE, a database of annotated comparative protein structure models.

Authors:  R Sánchez; U Pieper; N Mirković; P I de Bakker; E Wittenstein; A Sali
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Evaluation of PSI-BLAST alignment accuracy in comparison to structural alignments.

Authors:  I Friedberg; T Kaplan; H Margalit
Journal:  Protein Sci       Date:  2000-11       Impact factor: 6.725

3.  LiveBench-1: continuous benchmarking of protein structure prediction servers.

Authors:  J M Bujnicki; A Elofsson; D Fischer; L Rychlewski
Journal:  Protein Sci       Date:  2001-02       Impact factor: 6.725

4.  Mutations of acidic residues in RAG1 define the active site of the V(D)J recombinase.

Authors:  D R Kim; Y Dai; C L Mundy; W Yang; M A Oettinger
Journal:  Genes Dev       Date:  1999-12-01       Impact factor: 11.361

5.  Estimating the probability for a protein to have a new fold: A statistical computational model.

Authors:  E Portugaly; M Linial
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

6.  Modeling of loops in protein structures.

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

7.  Motif-based fold assignment.

Authors:  L Salwinski; D Eisenberg
Journal:  Protein Sci       Date:  2001-12       Impact factor: 6.725

8.  Improved recognition of native-like protein structures using a family of designed sequences.

Authors:  Patrice Koehl; Michael Levitt
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-08       Impact factor: 11.205

9.  Bub3 interaction with Mad2, Mad3 and Cdc20 is mediated by WD40 repeats and does not require intact kinetochores.

Authors:  R Fraschini; A Beretta; L Sironi; A Musacchio; G Lucchini; S Piatti
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

10.  Statistical potentials for fold assessment.

Authors:  Francisco Melo; Roberto Sánchez; Andrej Sali
Journal:  Protein Sci       Date:  2002-02       Impact factor: 6.725

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