<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/SRR336/051/SRR33638151/SRR33638151.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/044/SRR33638144/SRR33638144.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/046/SRR33638146/SRR33638146.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/045/SRR33638145/SRR33638145.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/050/SRR33638150/SRR33638150.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/047/SRR33638147/SRR33638147.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/043/SRR33638143/SRR33638143.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/052/SRR33638152/SRR33638152.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/048/SRR33638148/SRR33638148.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/054/SRR33638154/SRR33638154.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/049/SRR33638149/SRR33638149.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR336/053/SRR33638153/SRR33638153.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>New England Biolabs Inc.</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1265467</full_dataset_link><long_description>This work aims to solve the age-old mystery of the physiological target of the OLD (overcoming lysogenization defect) nuclease of phage P2, which interferes with the replication of phage Lambda in P2 lysogens. We screened a library of 245 unique phage-encoded tRNAs in E. coli MG1655 engineered to recapitulate the growth defect induced by P2-OLD. To identify rescue tRNAs, next-generation sequencing was run on cells transformed with the phage tRNA library before ("input") and after activation of P2-OLD ("output").</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>ATPase-powered antiphage nuclease with tRNA stem-severing activity</description><dates><last_updated>2025-05-22</last_updated><first_public>2025-05-22</first_public></dates><accession>PRJNA1265467</accession><cross_references/></HashMap>