Keap1 Recruits Neh2 through Binding to ETGE and DLG Motifs: Characterization of the Two-Site Molecular Recognition Model
University of Tsukuba · Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA) · +2 more institutions
Abstract
The expression of the phase 2 detoxification enzymes and antioxidant proteins is induced at the transcriptional level by Nrf2 and negatively regulated at the posttranslational level by Keap1 through protein-protein interactions with and subsequent proteolysis of Nrf2. We found that the Neh2 domain of Nrf2 is an intrinsically disordered but biologically active regulatory domain containing a 33-residue central alpha-helix followed by a mini antiparallel beta-sheet. Isothermal calorimetry analysis indicated that one Neh2 molecule interacts with two molecules of Keap1 via two binding sites, the stronger binding ETGE motif and the weaker binding DLG motif. Nuclear magnetic resonance titration study showed that…
Citation impact
- FWCI
- 7.09
- Percentile
- 100%
- References
- 71
Authors
6- KIKit I. Tong
University of Tsukuba, Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), Comprehensive Clinical Research
- YKYasutake Katoh
Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), Comprehensive Clinical Research, University of Tsukuba
- HKHideki Kusunoki
Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA)
- KIKen Itoh
Comprehensive Clinical Research, University of Tsukuba, Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA)
- TTToshiyuki TanakaCorresponding
Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), Life University
Topics & keywords
- Isothermal titration calorimetry
- Biology
- Binding site
- KEAP1
- Plasma protein binding
- Signal transducing adaptor protein
- Antiparallel (mathematics)
- Structural motif