Cargando…
DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities
Werner protein (WRN), member of the RecQ helicase family, is a helicase and exonuclease, and participates in multiple DNA metabolic processes including DNA replication, recombination and DNA repair. Mutations in the WRN gene cause Werner syndrome, associated with premature aging, genome instability...
Autores principales: | Tadokoro, Takashi, Kulikowicz, Tomasz, Dawut, Lale, Croteau, Deborah L., Bohr, Vilhelm A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409678/ https://www.ncbi.nlm.nih.gov/pubmed/22713343 |
Ejemplares similares
-
CDK2 phosphorylation of Werner protein (WRN) contributes to WRN’s DNA double‐strand break repair pathway choice
por: Lee, Jong‐Hyuk, et al.
Publicado: (2021) -
Recent Advances in Understanding Werner Syndrome
por: Shamanna, Raghavendra A., et al.
Publicado: (2017) -
A high-throughput screen to identify novel small molecule inhibitors of the Werner Syndrome Helicase-Nuclease (WRN)
por: Sommers, Joshua A., et al.
Publicado: (2019) -
RECQL5 cooperates with Topoisomerase II alpha in DNA decatenation and cell cycle progression
por: Ramamoorthy, Mahesh, et al.
Publicado: (2012) -
Werner syndrome protein works as a dimer for unwinding and replication fork regression
por: Shin, Soochul, et al.
Publicado: (2022)