<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR320/DRR320431/DRR320431_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR320/DRR320431/DRR320431_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><strain>BW25113</strain><omics_type>Genomics</omics_type><center_name>Graduate School of Engineering, The University of Tokyo</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJDB12336</full_dataset_link><scientific_name>Escherichia coli BW25113</scientific_name><long_description>In the early stage of translation elongation, peptidyl-tRNA (pep-tRNA) with short nascent chain frequently dissociates from the ribosome (pep-tRNA drop-off). Inactivation of PTH (peptidyl-tRNA hydrolase) causes rapid accumulation of pep-tRNAs and depletion of aminoacyl(aa)-tRNAs, leading to defective protein synthesis. We established a highly sensitive method for direct profiling of pep-tRNAs accumulated in the cell and identified more than 700 peptide sequences of the pep-tRNAs. In this experiment, to examine the involvement of RRF in pep-tRNA drop-off in the early elongation stage, we performed ribosome profiling of WT and temperature-sensitive RRF strain incubated at 43Â°C for 30 min.</long_description><tag>pathogen:priority</tag><tag>pathogen:bacterium</tag><tag>pathogen</tag><classification>bacteria</classification><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Escherichia coli BW25113</name><description>Ribosome profiling analyses on WT and RRFTs strain</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-05-21</first_public></dates><accession>PRJDB12336</accession><cross_references><taxon>679895</taxon></cross_references></HashMap>