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Identification of a rhodanese-like protein involved in thiouridine biosynthesis in Thermus thermophilus tRNA.
Shigi, Naoki; Asai, Shin-Ichi; Watanabe, Kimitsuna.
Afiliación
  • Shigi N; Biotechnology Research Institute for Drug Discovery, National Institute of Advanced Industrial Science and Technology (AIST), Tokyo, Japan.
  • Asai SI; Japan Biological Information Research Center (JBIRC), Japan Biological Informatics Consortium (JBIC), Tokyo, Japan.
  • Watanabe K; Biomedicinal Information Research Center (BIRC), National Institute of Advanced Industrial Science and Technology (AIST), Tokyo, Japan.
FEBS Lett ; 590(24): 4628-4637, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27878988
ABSTRACT
Incorporation of a sulfur atom into 2-thioribothymidine (s2 T or 5-methyl-2-thiouridine) at position 54 in thermophile tRNA is accomplished by an elaborate system composed of many proteins which confers thermostability to the translation system. We identified ttuD (tRNA-two-thiouridine D) as a gene for the synthesis of s2 T54 in Thermus thermophilus. The rhodanese-like protein TtuD enhances the activity of cysteine desulfurases and receives the persulfide generated by cysteine desulfurases in vitro. TtuD also enhances the formation of thiocarboxylated TtuB, the sulfur donor for the tRNA sulfurtransferase TtuA. Since cysteine desulfurases are the first enzymes in the synthesis of s2 T and other sulfur-containing compounds, TtuD has a role to direct sulfur flow to s2 T synthesis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sulfurtransferasas / Tiouridina / Proteínas Bacterianas / ARN de Transferencia / Thermus thermophilus Tipo de estudio: Diagnostic_studies Idioma: En Revista: FEBS Lett Año: 2016 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sulfurtransferasas / Tiouridina / Proteínas Bacterianas / ARN de Transferencia / Thermus thermophilus Tipo de estudio: Diagnostic_studies Idioma: En Revista: FEBS Lett Año: 2016 Tipo del documento: Article País de afiliación: Japón