Literature DB >> 8759004

PairWise and SearchWise: finding the optimal alignment in a simultaneous comparison of a protein profile against all DNA translation frames.

E Birney1, J D Thompson, T J Gibson.   

Abstract

DNA translation frames can be disrupted for several reasons, including: (i) errors in sequence determination; (ii) RNA processing, such as intron removal and guide RNA editing; (iii) less commonly, polymerase frameshifting during transcription or ribosomal frameshifting during translation. Frameshifts frequently confound computational activities involving homologous sequences, such as database searches and inferences on structure, function or phylogeny made from multiple alignments. A dynamic alignment algorithm is reported here which compares a protein profile (a residue scoring matrix for one or more aligned sequences) against the three translation frames of a DNA strand, allowing frameshifting. The algorithm has been incorporated into a new package, WiseTools, for comparison of biological sequences. A protein profile can be compared against either a DNA sequence or a protein sequence. The program PairWise may be used interactively for alignment of any two sequence inputs. SearchWise can perform combinations of searches through DNA or protein databases by a protein profile or DNA sequence. Routine application of the programs has revealed a set of database entries with frameshifts caused by errors in sequence determination.

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Year:  1996        PMID: 8759004      PMCID: PMC145991          DOI: 10.1093/nar/24.14.2730

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  43 in total

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Journal:  Nucleic Acids Res       Date:  1994-09       Impact factor: 16.971

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Authors:  T J Gibson; M Hyvönen; A Musacchio; M Saraste; E Birney
Journal:  Trends Biochem Sci       Date:  1994-09       Impact factor: 13.807

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  45 in total

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6.  A recent polyploidy superimposed on older large-scale duplications in the Arabidopsis genome.

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9.  Novel domains in NADPH oxidase subunits, sorting nexins, and PtdIns 3-kinases: binding partners of SH3 domains?

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10.  Complex genomic rearrangements lead to novel primate gene function.

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