EventsMOL2NET'15, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 1st ed.
Published
This submission belongs to the session 01. CHEMBIO.INFO-01: Cheminfo., Chemom., Comput. Quantum Chem. & Bioinfo. Congress, Cambridge, UK-Chapel Hill and Richmond, USA, 2015 of the event MOL2NET'15, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 1st ed.
Published date
04 Dec, 2015
Citation
Miguel de Sousa, Cristian Robert Munteanu, Alexandre Lopes Magalhães, Prot-SSP: a tool for amino acid pairing pattern analysis in secondary structures, in Proceedings of MOL2NET'15, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 1st ed., 5 December–15 December 2015, MDPI: Basel, Switzerland, doi: 10.3390/MOL2NET-1-F010
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Prot-SSP: a tool for amino acid pairing pattern analysis in secondary structures

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1. UCIBIO/REQUIMTE/University of Porto, R. Campo Alegre 687, 4169-007 Porto, Portugal
2. RNASA-IMEDIR group, Computer Science Faculty, University of A Coruna, Campus de Elviña S/N, 15071, A Coruña, Spain (Department of Information and Communication Technologies)
Abstract

It is known that individual amino acids can have a decisive role in the stabilization of a protein structure. Moreover, it is likely that specific amino acid combinations also fulfil structural and stabilizing roles in protein structure. We present Prot-SSP, an analytical Python tool designed to gather and parse sequence and structural data from sets of PDB files and determine amino acid residue pairing propensities and correlations in alpha helices and beta strands, in various secondary structure contexts. This versatile and user-friendly bioinformatic tool has proven useful for the analysis of a selected set of protein structures as shown in an illustrative example.

Keywords
secondary structure
amino acid pair
alpha helix
beta strand
software
Manuscript
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