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Structure of the Keap1:Nrf2 interface provides mechanistic insight into Nrf2 signaling
Open accessAbstract
Keap1 is a BTB-Kelch substrate adaptor protein that regulates steady-state levels of Nrf2, a bZIP transcription factor, in response to oxidative stress. We have determined the structure of the Kelch domain of Keap1 bound to a 16-mer peptide from Nrf2 containing a highly conserved DxETGE motif. The Nrf2 peptide contains two short antiparallel beta-strands connected by two overlapping type I beta-turns stabilized by the aspartate and threonine residues. The beta-turn region fits into a binding pocket on the top face of the Kelch domain and the glutamate residues form multiple hydrogen bonds with highly conserved residues in Keap1. Mutagenesis experiments confirmed the role of individual amino acids for binding of Nrf2 to Keap1 and for Keap1-mediated repression of Nrf2-dependent gene expression. Our results provide a detailed picture of how a BTB-Kelch substrate adaptor protein binds to its cognate substrate and will enable the rational design of novel chemopreventive agents.
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“Crystal structures of peptide substrate complexes have been reported for four BTB-Kelch family members, including KEAP1, KLHL2, KLHL3 and KLHL20 (refs 80,81,82 ).”
From Targeted protein degradation: expanding the toolbox (2019) · cites this paper as [80]
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InfluentialChen, T., Ma, J., Sheng, Y., Cao, S., Liu, H., Yan, J., Yang, H., Qi, X., & Shi, Q. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108954 · Cited by 1
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“The crystal structure of the Keap1 Kelch domain (PDB ID: 2FLU; Lo et al., 2006) was retrieved from the RCSB Protein Data Bank and prepared using the Protein Preparation Wizard (Madhavi Sastry et al., 2013).”
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“Molecular docking studies have shown CGA may bind to Keap1 residues associated with Nrf2, such as ARG-415, with a minimum molecular affinity of -9.2 kcal/mol [28].”
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“Models trained on STARMAP-defined regions achieved high predictive performance, with the KEAP1-NRF2 interaction among the strongest and most confident associations (Log odds = 5.000, Fig.”
InfluentialJin, Y., Zhang, J. F., Miao, J., Peng, Z., Liu, Y., & Zhao, Z. (2026) · Food Chemistry X · doi:10.1016/j.fochx.2026.103962
“The DEETGE motif is recognized as the high-affinity sequence for the Kelch domain of Keap1 (Begnini et al., 2020; Lo et al., 2006).”
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“4A), which aligns with the finding of a previous study [ 52 ].”
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“…mutations, in contrast, are almost exclusively confined to the DLG and ETGE motifs of Neh2 [65,66], with R34, D29, W24, L30, D77, E79, T80, and E82 emerging as recurrent residues—precisely the residues that crystal structures predict to be critical for KEAP1 Kelch-pocket engagement [51,52].”
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“Arg415, Arg483 and Ser508 contribute to recognition in the P1 region, while Ser363, Arg380 and Asn382 participate in the adjacent P2 region (Jiang et al. 2014 ; Lo et al. 2006).”
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“Since ARG-415 is a critical anchoring residue that binds the ETGE motif of NRF2 [62], this spatial overlap suggests a structural basis for competitive inhibition.”
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“The crystal structure of KEAP1 was obtained from the Protein Data Bank (PDB ID: 2FLU) [27].”
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“However, the endogenous Nrf2-ETGE motif binds Keap1 with high affinity (5–20 nM, equivalent to approximately −11.3 kcal/mol) [32,33].”
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“Both complexes reported single digit to low double digit nM affinity (Tong et al., 2006; Lo et al., 2006; Eggler et al., 2005; Gong et al., 2016).”
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Metadata
- Authors
- Lo, S., Li, X., Henzl, M. T., Beamer, L. J., & Hannink, M.
- Affiliations
- University of Missouri (US)
- Corresponding author
- Beamer, Lesa J
- Hannink, Mark
- Venue
- The EMBO Journal
- Published
- 2006-08-03
- Volume
- 25
- Issue
- 15
- Pages
- 3605-3617
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC1538563
- OpenAlex
- W2141982524
- Cited by
- 604
- References
- 68
- Citations by year
- 2026: 66 · 2025: 66 · 2024: 44 · 2023: 48 · 2022: 47 · 2021: 36 · 2020: 35 · 2019: 23 · 2018: 22 · 2017: 21 · 2016: 25 · 2015: 25 · 2014: 22 · 2013: 34 · 2012: 22
- FWCI
- 4.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (P50CA103130)
- National Center for Complementary and Integrative Health (AT003899, R01AT003899)
- Lawrence Berkeley National Laboratory
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- Keap1, Nrf2, Kelch domain, protein-protein interaction, beta-turn, oxidative stress response, chemoprevention, protein structure
- MeSH terms
- Kelch-Like ECH-Associated Protein 1, Amino Acid Sequence, Animals, Binding Sites, Cells, Cultured, Chlorocebus aethiops, Humans, Models, Molecular, Molecular Sequence Data, Phosphorylation, Protein Binding, Protein Conformation, Signal Transduction, Conserved Sequence, Protein Structure, Tertiary, Dimerization, COS Cells, Amino Acid Motifs, Intracellular Signaling Peptides and Proteins, NF-E2-Related Factor 2
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