A divalent FHA/BRCT‐binding mechanism couples the MRE11–RAD50–NBS1 complex to damaged chromatin-Reference-Cited by-同舟云学术

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A divalent FHA/BRCT‐binding mechanism couples the MRE11–RAD50–NBS1 complex to damaged chromatin

Published:2010-03-12 Issue:5 Volume:11 Page:387-392
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Hari Flurina J¹,Spycher Christoph¹,Jungmichel Stephanie¹,Pavic Lucijana¹,Stucki Manuel¹

Affiliation:

1. Institute of Veterinary Biochemistry and Molecular Biology, University of Zurich Winterthurerstrasse 190 Zurich 8057 Switzerland

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1038/embor.2010.30

Reference22 articles.

1. Detection of a tandem BRCT in Nbs1 and Xrs2 with functional implications in the DNA damage response

2. Nibrin Forkhead-associated Domain and Breast Cancer C-terminal Domain Are Both Required for Nuclear Focus Formation and Phosphorylation

3. Phospho‐dependent interactions between NBS1 and MDC1 mediate chromatin retention of the MRN complex at sites of DNA damage

4. The MRE11 complex: at the crossroads of DNA repair and checkpoint signalling

5. The NBS1-ATM Connection Revisited

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1. Identification of plants’ functional counterpart of the metazoan mediator of DNA Damage checkpoint 1;EMBO Reports;2024-03-04

2. The immediate-early protein 1 of human herpesvirus 6B interacts with NBS1 and inhibits ATM signaling;EMBO Reports;2024-01-02

3. The molecular details of a novel phosphorylation‐dependent interaction between MRN and the SOSS complex;Protein Science;2023-09-26

4. Identification of plants functional counterparts of the metazoan Mediator of DNA Damage Checkpoint 1;2023-05-19

5. Species variations in XRCC1 recruitment strategies for FHA domain-containing proteins;DNA Repair;2022-02

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