Skip Navigation

This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (11)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Errami, M.
Right arrow Articles by Deléage, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Errami, M.
Right arrow Articles by Deléage, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics Vol. 19 no. 4 2003
Pages 506-512
© 2003 Oxford University Press

Detection of unrelated proteins in sequences multiple alignments by using predicted secondary structures

Mounir Errami , Christophe Geourjon and Gilbert Deléage *

Pôle de BioInformatique Lyonnais, Institut de Biologie et de Chimie des Protéines, Centre National de la Recherche Scientifique, UMR 5086, 69367 Lyon CEDEX 07, France

Received on March 14, 2002 ; revised on August 26, 2002 ; accepted on October 8, 2002

Motivation: Multiple sequence alignments are essential tools for establishing the homology relations between proteins. Essential amino acids for the function and/or the structure are generally conserved, thus providing key arguments to help in protein characterization. However for distant proteins, it is more difficult to establish, in a reliable way, the homology relations that may exist between them. In this article, we show that secondary structure prediction is a valuable way to validate protein families at low identity rate.

Results: We show that the analysis of the secondary structures compatibility is a reliable way to discard non-related proteins in low identity multiple alignment.

Availability: This validation is possible through our NPS@ server (http://npsa-pbil.ibcp.fr)

Contact: g.deleage{at}ibcp.fr

* To whom correspondence should be addressed.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Brief BioinformHome page
S. J. Sammut, R. D. Finn, and A. Bateman
Pfam 10 years on: 10 000 families and still growing
Brief Bioinform, May 1, 2008; 9(3): 210 - 219.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
J. D. Thompson, V. Prigent, and O. Poch
LEON: multiple aLignment Evaluation Of Neighbours
Nucleic Acids Res., February 24, 2004; 32(4): 1298 - 1307.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.