Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 5 of 5 for “"SBP1"”.
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Identification and stoichiometric analysis of the monosomal translational complex
… proteins shown to be present in the 77S complex: SBP1, SLF1, PUB1, SUP35, SUP45 and SSD1. By comparing the ratios of AU-FDS/A230, I found only 56% of monosomal complexes contained eIF4E and only 34% contained eIF4G during translation elongation, implying that not all 77S complexes were in the …
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The Role of Endogenous Arabidopsis Proteins In Rna Silencing and Hc-Pro-Mediated Suppression of Silencing
… interacts with S-RIBONUCLEASE BINDING PROTEIN (SBP1), a RING-HC domain E3 ubiquitin ligase, which in turn also interacts with another endogenous suppressor of silencing, a transcription factor called RAV2. SBP1 is required for complete suppression of RNA silencing by HC-Pro and over-expression …
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Multilayered regulation of translation: roles of rRNA modifications, alternative initiation factors, and RNA-binding proteins
… the intrinsically disordered RNA-binding protein Sbp1 is examined for its role in translational regulation and mRNA storage. Our findings indicate that Sbp1 modulates translation efficiency and participates in mRNA sequestration into ribonucleoprotein granules, influencing cellular responses to …
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Identifying novel proteins in translation complex by using analytical ultracentrifugation with fluorescent detection system
… we were able to identify at five new proteins, SBP1, SLF1, PUB1, SUP35 and SSD1 as being part of this complex. SBP1 had previously been shown to be a component of stress granules formed following glucose depletion and SLF1 to be associated with translational process. PUB1 could bind to ARE and …
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Identification and characterization of novel genes involved in DNA double strand break repair process in the yeast Saccharomyces cerevisiae
… these genes, PPH3/PSY2, HUR1, BUB1/BUB2, and SBP1 were selected for follow up experiments. Small-scale plasmid repair and chromosomal break repair assays were used to verify the involvement of these selected candidates in the efficiency of NHEJ. Deletion of any one of the above selected genes …