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Multicomponent assemblies in DNA-double-strand break repair by NHEJ.
Hnízda, Ales; Blundell, Tom L.
Afiliação
  • Hnízda A; Department of Biochemistry, University of Cambridge, Tennis Court Rd., Cambridge, CB2 1GA, UK. Electronic address: ah960@cam.ac.uk.
  • Blundell TL; Department of Biochemistry, University of Cambridge, Tennis Court Rd., Cambridge, CB2 1GA, UK. Electronic address: tlb20@cam.ac.uk.
Curr Opin Struct Biol ; 55: 154-160, 2019 04.
Article em En | MEDLINE | ID: mdl-31125797
Non-homologous end joining (NHEJ), a process for repair of DNA-breaks that does not require a DNA-template, involves synapsis, end-processing and ligation. Synapsis is initiated by assembly of the Ku-heterodimer on DNA broken ends, followed by the formation of DNA-dependent protein kinase (DNA-PK) - an assembly of the catalytic subunit (DNA-PKcs), the Ku-heterodimer and DNA. Recent progress in understanding the structural architecture of DNA-PK, achieved by X-ray crystallography and cryo-electron microscopy, has revealed a stage of DNA-PKcs on which other components from the pathway assemble and mediate kinase activity allosterically. This review provides a comparative overview of recently published structures of DNA-PK, together with a discussion of other complexes mediated by the Ku heterodimer. It also shows that some binders are specific to particular patho-physiological conditions.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Substâncias Macromoleculares / Proteína Quinase Ativada por DNA / Autoantígeno Ku Limite: Humans Idioma: En Revista: Curr Opin Struct Biol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Substâncias Macromoleculares / Proteína Quinase Ativada por DNA / Autoantígeno Ku Limite: Humans Idioma: En Revista: Curr Opin Struct Biol Ano de publicação: 2019 Tipo de documento: Article