Processive incorporation of multiple selenocysteine residues is driven by a novel feature of the selenocysteine insertion sequence
Author:
Funder
HHS | National Institutes of Health (NIH)
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference40 articles.
1. Recognition of UGA as a selenocysteine codon in type I deiodinase requires sequences in the 3′ untranslated region;Berry;Nature,1991
2. Characterization of mSelB, a novel mammalian elongation factor for selenoprotein translation;Fagegaltier;EMBO J,2000
3. Decoding apparatus for eukaryotic selenocysteine insertion;Tujebajeva;EMBO Rep,2000
4. Identification of a selenocysteyl-tRNA(Ser) in mammalian cells that recognizes the nonsense codon, UGA;Lee;J. Biol. Chem,1989
5. A novel RNA binding protein, SBP2, is required for the translation of mammalian selenoprotein mRNAs;Copeland;EMBO J,2000
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