Cargando…
Structural mechanism of the phosphorylation-dependent dimerization of the MDC1 forkhead-associated domain
MDC1 is a key mediator of the DNA-damage response in mammals with several phosphorylation-dependent protein interaction domains. The function of its N-terminal forkhead-associated (FHA) domain remains elusive. Here, we show with structural, biochemical and cellular data that the FHA domain mediates...
Autores principales: | Liu, Jinping, Luo, Shukun, Zhao, Hongchang, Liao, Ji, Li, Jing, Yang, Chunying, Xu, Bo, Stern, David F., Xu, Xingzhi, Ye, Keqiong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351156/ https://www.ncbi.nlm.nih.gov/pubmed/22234877 http://dx.doi.org/10.1093/nar/gkr1296 |
Ejemplares similares
-
The molecular basis of ATM-dependent dimerization of the Mdc1 DNA damage checkpoint mediator
por: Jungmichel, Stephanie, et al.
Publicado: (2012) -
CK2 phosphorylation-dependent interaction between aprataxin and MDC1 in the DNA damage response
por: Becherel, Olivier J., et al.
Publicado: (2010) -
Modulation of LSD1 phosphorylation by CK2/WIP1 regulates RNF168-dependent 53BP1 recruitment in response to DNA damage
por: Peng, Bin, et al.
Publicado: (2015) -
HERC2/USP20 coordinates CHK1 activation by modulating CLASPIN stability
por: Zhu, Min, et al.
Publicado: (2014) -
Oocytes can repair DNA damage during meiosis via a microtubule-dependent recruitment of CIP2A–MDC1–TOPBP1 complex from spindle pole to chromosomes
por: Leem, Jiyeon, et al.
Publicado: (2023)