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pubmed-article:9419243pubmed:abstractTextSequence similarity has given rise to the proposal that IF-2, EF-G, and EF-Tu are related through a common ancestor. We evaluate this proposition and whether the relationship can be extended to other factors of protein synthesis. Analysis of amino acid sequence similarity gives statistical support for an evolutionary affiliation among IF-1, IF-2, IF-3, EF-Tu, EF-Ts, and EF-G and suggests further that this association is a result of gene duplication/fusion events. In support of this mechanism, the three-dimensional structures of IF-3, EF-Tu, and EF-G display a predictable domain structure and overall conformational similarity. The model that we propose consists of three consecutives duplication/fusion events which would have taken place before the divergence of the three superkingdoms: eubacteria, archaea, and eukaryotes. The root of this protein superfamily tree would be an ancestor of the modern IF-1 gene sequence. The repeated fundamental motif of this protein superfamily is a small RNA binding domain composed of two alpha-helices packed along side of an antiparallel beta-sheet.lld:pubmed
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pubmed-article:9419243pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9419243pubmed:articleTitleOn the origin of protein synthesis factors: a gene duplication/fusion model.lld:pubmed
pubmed-article:9419243pubmed:affiliationDépartement de biochimie, Université de Montréal, Québec, Canada.lld:pubmed
pubmed-article:9419243pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9419243pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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