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Everything OLD is new again: How structural, functional, and bioinformatic advances have redefined a neglected nuclease family.
Dot, Elena Wanvig; Thomason, Lynn C; Chappie, Joshua S.
Afiliación
  • Dot EW; Department of Molecular Medicine, Cornell University, Ithaca, New York, USA.
  • Thomason LC; Molecular Control and Genetics Section, RNA Biology Laboratory, National Cancer Institute at Frederick, National Institutes of Health, Frederick, Maryland, USA.
  • Chappie JS; Department of Molecular Medicine, Cornell University, Ithaca, New York, USA.
Mol Microbiol ; 120(2): 122-140, 2023 08.
Article en En | MEDLINE | ID: mdl-37254295
Overcoming lysogenization defect (OLD) proteins are a conserved family of ATP-powered nucleases that function in anti-phage defense. Recent bioinformatic, genetic, and crystallographic studies have yielded new insights into the structure, function, and evolution of these enzymes. Here we review these developments and propose a new classification scheme to categorize OLD homologs that relies on gene neighborhoods, biochemical properties, domain organization, and catalytic machinery. This taxonomy reveals important similarities and differences between family members and provides a blueprint to contextualize future in vivo and in vitro findings. We also detail how OLD nucleases are related to PARIS and Septu anti-phage defense systems and discuss important mechanistic questions that remain unanswered.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacterias / Bacteriófagos / Esterasas Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacterias / Bacteriófagos / Esterasas Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos