<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Martin Garrido N</submitter><funding>Royal Society</funding><funding>Wellcome Trust</funding><pagination>168713</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7618050</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>436(18)</volume><pubmed_abstract>Bacteriophage ΦKZ (PhiKZ) is the founding member of a family of giant bacterial viruses. It has potential as a therapeutic as its host, Pseudomonas aeruginosa, kills tens of thousands of people worldwide each year. ΦKZ infection is independent of the host transcriptional apparatus; the virus forms a "nucleus", producing a proteinaceous barrier around the ΦKZ genome that excludes the host immune systems. It expresses its own non-canonical multi-subunit non-virion RNA polymerase (nvRNAP), which is imported into its "nucleus" to transcribe viral genes. The ΦKZ nvRNAP is formed by four polypeptides representing homologues of the eubacterial β/β' subunits, and a fifth that is likely to have evolved from an ancestral homologue to σ-factor. We have resolved the structure of the ΦKZ nvRNAP initiat</pubmed_abstract><journal>Journal of molecular biology</journal><pubmed_title>Structure of the Bacteriophage PhiKZ Non-virion RNA Polymerase Transcribing from its Promoter p119L.</pubmed_title><pmcid>PMC7618050</pmcid><funding_grant_id>206212/Z/17/A</funding_grant_id><funding_grant_id>206212</funding_grant_id><funding_grant_id>206212/Z/17/Z</funding_grant_id><pubmed_authors>Yakunina M</pubmed_authors><pubmed_authors>de Martin Garrido N</pubmed_authors><pubmed_authors>Ramlaul K</pubmed_authors><pubmed_authors>Chen CS</pubmed_authors><pubmed_authors>Aylett CHS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure of the Bacteriophage PhiKZ Non-virion RNA Polymerase Transcribing from its Promoter p119L.</name><description>Bacteriophage ΦKZ (PhiKZ) is the founding member of a family of giant bacterial viruses. It has potential as a therapeutic as its host, Pseudomonas aeruginosa, kills tens of thousands of people worldwide each year. ΦKZ infection is independent of the host transcriptional apparatus; the virus forms a "nucleus", producing a proteinaceous barrier around the ΦKZ genome that excludes the host immune systems. It expresses its own non-canonical multi-subunit non-virion RNA polymerase (nvRNAP), which is imported into its "nucleus" to transcribe viral genes. The ΦKZ nvRNAP is formed by four polypeptides representing homologues of the eubacterial β/β' subunits, and a fifth that is likely to have evolved from an ancestral homologue to σ-factor. We have resolved the structure of the ΦKZ nvRNAP initiat</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-06-06T00:29:35.11Z</modification><creation>2026-05-24T03:11:38.305Z</creation></dates><accession>S-EPMC7618050</accession><cross_references><pubmed>39029888</pubmed><doi>10.1016/j.jmb.2024.168713</doi></cross_references></HashMap>