BRCT Repeats As Phosphopeptide-Binding Modules Involved in Protein Targeting
Center for Cancer Research · Massachusetts Institute of Technology
Abstract
We used a proteomic approach to identify phosphopeptide-binding modules mediating signal transduction events in the DNA damage response pathway. Using a library of partially degenerate phosphopeptides, we identified tandem BRCT (BRCA1 carboxyl-terminal) domains in PTIP (Pax transactivation domain-interacting protein) and in BRCA1 as phosphoserine- or phosphothreonine-specific binding modules that recognize substrates phosphorylated by the kinases ATM (ataxia telangiectasia-mutated) and ATR (ataxia telangiectasia- and RAD3-related) in response to gamma-irradiation. PTIP tandem BRCT domains are responsible for phosphorylation-dependent protein localization into 53BP1- and phospho-H2AX (gamma-H2AX)-containing…
Citation impact
- FWCI
- 18.67
- Percentile
- 100%
- References
- 23
Authors
4- IAIsaac A. MankeCorresponding
Center for Cancer Research, Massachusetts Institute of Technology
- DMDrew M. Lowery
Center for Cancer Research, Massachusetts Institute of Technology
- ANAnhco Nguyen
Center for Cancer Research, Massachusetts Institute of Technology
- MBMichael B. Yaffe
Center for Cancer Research, Massachusetts Institute of Technology
Topics & keywords
- Phosphopeptide
- Phosphoserine
- Phosphorylation
- DNA damage
- Cell biology
- Biology
- Nuclear protein
- Transactivation
- Good health and well-being