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Structural basis for AcrVA4 inhibition of specific CRISPR-Cas12a.
Knott, Gavin J; Cress, Brady F; Liu, Jun-Jie; Thornton, Brittney W; Lew, Rachel J; Al-Shayeb, Basem; Rosenberg, Daniel J; Hammel, Michal; Adler, Benjamin A; Lobba, Marco J; Xu, Michael; Arkin, Adam P; Fellmann, Christof; Doudna, Jennifer A.
Afiliação
  • Knott GJ; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
  • Cress BF; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
  • Liu JJ; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
  • Thornton BW; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
  • Lew RJ; Gladstone Institutes, San Francisco, United States.
  • Al-Shayeb B; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, United States.
  • Rosenberg DJ; Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, United States.
  • Hammel M; Graduate Group in Biophysics, University of California, Berkeley, Berkeley, United States.
  • Adler BA; Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, United States.
  • Lobba MJ; UC Berkeley-UCSF Graduate Program in Bioengineering, University of California, Berkeley, Berkeley, United States.
  • Xu M; Department of Bioengineering, University of California, Berkeley, Berkeley, United States.
  • Arkin AP; Department of Chemistry, University of California, Berkeley, Berkeley, United States.
  • Fellmann C; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
  • Doudna JA; Department of Bioengineering, University of California, Berkeley, Berkeley, United States.
Elife ; 82019 08 09.
Article em En | MEDLINE | ID: mdl-31397669
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bacteriófagos / Proteínas Virais / Acidaminococcus / Inibidores Enzimáticos / Sistemas CRISPR-Cas / Clostridiales / Interações Hospedeiro-Parasita Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bacteriófagos / Proteínas Virais / Acidaminococcus / Inibidores Enzimáticos / Sistemas CRISPR-Cas / Clostridiales / Interações Hospedeiro-Parasita Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido