8ejr

Kelch domain of human KEAP1 bound to Nrf2 linear peptide, Ac-GDPETGE-NH2

Method: X-RAY DIFFRACTION Dmax: 91.8 Å Quality: GOOD

1. Protein Identity and Related Structures Protein Identity & Related Structures

Kelch-like ECH-associated protein 1

Homo sapiens

UniProt Q14145

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 312–624 Fragment:UNP residues 320-812 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;290 K;1.6 M ammonium sulfate, 100 mM Bis-Tris pH 6.5, 0.8% PEG monomethyl ether (MME) 550 Resolution 2.08 Å R-free 0.249
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 312–624 Fragment:UNP residues 320-812 Linear peptide from Nuclear factor erythroid 2-related factor 2 × 1 (Q16236) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;290 K;1.6 M ammonium sulfate, 100 mM Bis-Tris pH 6.5, 0.8% PEG monomethyl ether (MME) 550 Resolution 2.08 Å R-free 0.249

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

119 other PDB entries and 193 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KEAP1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 24–336; UniProt 312–624 Author chain B; PDBConstruct 24–336; UniProt 312–624

Linear peptide from Nuclear factor erythroid 2-related factor 2

OrganismNot specified

UniProt Q16236

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 76–82 Non-standard monomer:Yes (specific site not provided by mmCIF) Kelch-like ECH-associated protein 1 × 1 (Q14145) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;290 K;1.6 M ammonium sulfate, 100 mM Bis-Tris pH 6.5, 0.8% PEG monomethyl ether (MME) 550 Resolution 2.08 Å R-free 0.249

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

10 other PDB entries and 13 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NF2L2_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 2–8; UniProt 76–82

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 8ejr

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8ejr
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8ejr
Deposition date deposition_date2022-09-18
Structure title titleKelch domain of human KEAP1 bound to Nrf2 linear peptide, Ac-GDPETGE-NH2
Keywords keywordsProtein interaction, inhibitor, cyclic peptide, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier27.08
Radius of gyration Rg (electron density) rg_electron26.49
Forward intensity I(0) i070710200.00
Molecular weight molecular_weight62492.0 kDa
Excluded volume excluded_volume76720 ų
Envelope volume envelope_volume91510 ų
Hydration-shell volume shell_volume29188 ų
Envelope diameter envelope_diameter93.8
Shell Rg shell_rg33.37
Envelope Rg envelope_rg26.77
Shape Rg shape_rg26.50
Total Rg total_rg27.16
Total atoms total_atoms4392
Residues n_residues573
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax91.8
Rg (real space) rg_real27.18
Rg uncertainty (real space) rg_real_error0.71
I(0) (real space) i0_real7.0710e+07
I(0) uncertainty (real space) i0_real_error1.0960e+06
Rg (reciprocal space) rg_reciprocal27.15
I(0) (reciprocal space) i0_reciprocal70710000.0000
Solution quality estimate total_estimate0.8520
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary90.2
Skewness Skewness skewness0.450
Kurtosis Kurtosis kurtosis-0.361
Angular range angular_range— – 0.2950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16690000.0000
Real-space data points n_real_points60
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.764; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.897; Smooth: 0.884

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)