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De novo identification of highly diverged protein repeats by probabilistic consistency
Author(s) -
A. Biegert,
Johannes Söding
Publication year - 2008
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btn039
Subject(s) - probabilistic logic , executable , computational biology , tandem repeat , computer science , sequence alignment , sequence (biology) , multiple sequence alignment , biology , homology (biology) , hidden markov model , genetics , algorithm , genome , peptide sequence , artificial intelligence , gene , operating system
An estimated 25% of all eukaryotic proteins contain repeats, which underlines the importance of duplication for evolving new protein functions. Internal repeats often correspond to structural or functional units in proteins. Methods capable of identifying diverged repeated segments or domains at the sequence level can therefore assist in predicting domain structures, inferring hypotheses about function and mechanism, and investigating the evolution of proteins from smaller fragments.

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