ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

iPBA: a tool for protein structure comparison using sequence alignment strategies

Gelly, Jean-Christophe and Joseph, Agnel Praveen and Srinivasan, Narayanaswamy and de Brevern, Alexandre G (2011) iPBA: a tool for protein structure comparison using sequence alignment strategies. In: Nucleic Acids Research, 39 (2). W18-W23.

[img] PDF
iPBA.pdf - Published Version
Restricted to Registered users only

Download (15MB) | Request a copy
Official URL: http://nar.oxfordjournals.org/content/39/suppl_2/W...

Abstract

With the immense growth in the number of available protein structures, fast and accurate structure comparison has been essential. We propose an efficient method for structure comparison, based on a structural alphabet. Protein Blocks (PBs) is a widely used structural alphabet with 16 pentapeptide conformations that can fairly approximate a complete protein chain. Thus a 3D structure can be translated into a 1D sequence of PBs. With a simple Needleman-Wunsch approach and a raw PB substitution matrix, PB-based structural alignments were better than many popular methods. iPBA web server presents an improved alignment approach using (i) specialized PB Substitution Matrices (SM) and (ii) anchor-based alignment methodology. With these developments, the quality of similar to 88% of alignments was improved. iPBA alignments were also better than DALI, MUSTANG and GANGSTA(+) in > 80% of the cases. The webserver is designed to for both pairwise comparisons and database searches. Outputs are given as sequence alignment and superposed 3D structures displayed using PyMol and Jmol. A local alignment option for detecting subs-structural similarity is also embedded. As a fast and efficient `sequence-based' structure comparison tool, we believe that it will be quite useful to the scientific community. iPBA can be accessed at http://www.dsimb.inserm.fr/dsimb_tools/ipba/.

Item Type: Journal Article
Publication: Nucleic Acids Research
Publisher: Oxford University Press
Additional Information: Copyright of this article belongs to Oxford University Press.
Department/Centre: Division of Biological Sciences > Molecular Biophysics Unit
Date Deposited: 18 Jul 2011 09:43
Last Modified: 18 Jul 2011 09:43
URI: http://eprints.iisc.ac.in/id/eprint/39188

Actions (login required)

View Item View Item