4.7 Article

SECISaln, a web-based tool for the creation of structure-based alignments of eukaryotic SECIS elements

Journal

BIOINFORMATICS
Volume 25, Issue 5, Pages 674-675

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btp020

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Funding

  1. Spanish Ministry of Education and Science
  2. BioSapiens European Network of Excellence
  3. National Institute for Bioinformatics
  4. ACI BCMS of the French Ministry of Research
  5. Pre-doctoral Fellowship from the Spanish Ministry of Education and Science

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Selenoproteins contain the 21st amino acid selenocysteine which is encoded by an inframe UGA codon, usually read as a stop. In eukaryotes, its co-translational recoding requires the presence of an RNA stem-loop structure, the SECIS element in the 3 untranslated region of (UTR) selenoprotein mRNAs. Despite little sequence conservation, SECIS elements share the same overall secondary structure. Until recently, the lack of a significantly high number of selenoprotein mRNA sequences hampered the identification of other potential sequence conservation. In this work, the web-based tool SECISaln provides for the first time an extensive structure-based sequence alignment of SECIS elements resulting from the well-defined secondary structure of the SECIS RNA and the increased size of the eukaryotic selenoproteome. We have used SECISaln to improve our knowledge of SECIS secondary structure and to discover novel, conserved nucleotide positions and we believe it will be a useful tool for the selenoprotein and RNA scientific communities.

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