Characterization of Mammalian Selenoproteomes
In the genetic code, UGA serves as a stop signal and a selenocysteine codon, but no computational methods for identifying its coding function are available. Consequently, most selenoprotein genes are misannotated. We identified selenoprotein genes in sequenced mammalian genomes by methods that rely...
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Published in | Science (American Association for the Advancement of Science) Vol. 300; no. 5624; pp. 1439 - 1443 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Association for the Advancement of Science
30.05.2003
The American Association for the Advancement of Science |
Subjects | |
Online Access | Get full text |
ISSN | 0036-8075 1095-9203 1095-9203 |
DOI | 10.1126/science.1083516 |
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Summary: | In the genetic code, UGA serves as a stop signal and a selenocysteine codon, but no computational methods for identifying its coding function are available. Consequently, most selenoprotein genes are misannotated. We identified selenoprotein genes in sequenced mammalian genomes by methods that rely on identification of selenocysteine insertion RNA structures, the coding potential of UGA codons, and the presence of cysteine-containing homologs. The human selenoproteome consists of 25 selenoproteins. |
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Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-2 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0036-8075 1095-9203 1095-9203 |
DOI: | 10.1126/science.1083516 |