Literature DB >> 16020471

SPEM: improving multiple sequence alignment with sequence profiles and predicted secondary structures.

Hongyi Zhou1, Yaoqi Zhou.   

Abstract

MOTIVATION: Multiple sequence alignment is an essential part of bioinformatics tools for a genome-scale study of genes and their evolution relations. However, making an accurate alignment between remote homologs is challenging. Here, we develop a method, called SPEM, that aligns multiple sequences using pre-processed sequence profiles and predicted secondary structures for pairwise alignment, consistency-based scoring for refinement of the pairwise alignment and a progressive algorithm for final multiple alignment.
RESULTS: The alignment accuracy of SPEM is compared with those of established methods such as ClustalW, T-Coffee, MUSCLE, ProbCons and PRALINE(PSI) in easy (homologs) and hard (remote homologs) benchmarks. Results indicate that the average sum of pairwise alignment scores given by SPEM are 7-15% higher than those of the methods compared in aligning remote homologs (sequence identity <30%). Its accuracy for aligning homologs (sequence identity >30%) is statistically indistinguishable from those of the state-of-the-art techniques such as ProbCons or MUSCLE 6.0. AVAILABILITY: The SPEM server and its executables are available on http://theory.med.buffalo.edu.

Entities:  

Mesh:

Year:  2005        PMID: 16020471     DOI: 10.1093/bioinformatics/bti582

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  23 in total

1.  MSACompro: protein multiple sequence alignment using predicted secondary structure, solvent accessibility, and residue-residue contacts.

Authors:  Xin Deng; Jianlin Cheng
Journal:  BMC Bioinformatics       Date:  2011-12-14       Impact factor: 3.169

2.  Predicting Protein Model Quality from Sequence Alignments by Support Vector Machines.

Authors:  Xin Deng; Jilong Li; Jianlin Cheng
Journal:  J Proteomics Bioinform       Date:  2013-11-04

3.  Multiple sequence alignment by conformational space annealing.

Authors:  Keehyoung Joo; Jinwoo Lee; Ilsoo Kim; Sung Jong Lee; Jooyoung Lee
Journal:  Biophys J       Date:  2008-08-08       Impact factor: 4.033

4.  PROMALS3D: multiple protein sequence alignment enhanced with evolutionary and three-dimensional structural information.

Authors:  Jimin Pei; Nick V Grishin
Journal:  Methods Mol Biol       Date:  2014

5.  MULTICOM: a multi-level combination approach to protein structure prediction and its assessments in CASP8.

Authors:  Zheng Wang; Jesse Eickholt; Jianlin Cheng
Journal:  Bioinformatics       Date:  2010-02-11       Impact factor: 6.937

6.  Predicting continuous local structure and the effect of its substitution for secondary structure in fragment-free protein structure prediction.

Authors:  Eshel Faraggi; Yuedong Yang; Shesheng Zhang; Yaoqi Zhou
Journal:  Structure       Date:  2009-11-11       Impact factor: 5.006

7.  The MULTICOM toolbox for protein structure prediction.

Authors:  Jianlin Cheng; Jilong Li; Zheng Wang; Jesse Eickholt; Xin Deng
Journal:  BMC Bioinformatics       Date:  2012-04-30       Impact factor: 3.169

8.  Designing and benchmarking the MULTICOM protein structure prediction system.

Authors:  Jilong Li; Xin Deng; Jesse Eickholt; Jianlin Cheng
Journal:  BMC Struct Biol       Date:  2013-02-27

9.  Improving accuracy of multiple sequence alignment algorithms based on alignment of neighboring residues.

Authors:  Yue Lu; Sing-Hoi Sze
Journal:  Nucleic Acids Res       Date:  2008-12-04       Impact factor: 16.971

Review 10.  Upcoming challenges for multiple sequence alignment methods in the high-throughput era.

Authors:  Carsten Kemena; Cedric Notredame
Journal:  Bioinformatics       Date:  2009-07-30       Impact factor: 6.937

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