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Kelch domain of human KEAP1 bound to NRF2 peptide, ldeetgeal

Analyse Kelch domain of human KEAP1 bound to NRF2 peptide, ldeetgeal in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7K29
Type
protein
Length
582 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kelch-like ech-associated protein 1; ACE-leu-asp-glu-glu-thr-gly-glu-ala-leu-NH2
UniProt
Q14145
Ligands
ACE, SO4, NH2
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 3 distinct chains · 0% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKelch-like ech-associated protein 1protein2830% helix, 50% strandQ14145
BKelch-like ech-associated protein 1protein2900% helix, 51% strandQ14145
PACE-leu-asp-glu-glu-thr-gly-glu-ala-leu-NH2protein90% helix, 0% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains P
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B, P
  • NH2 · Amino group · ion · chains A, P

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16040.760.8361empty
24450.710.8243empty
31320.560.8327empty
4690.440.8115empty
51430.410.7424empty

Interfaces

2 interfaces between chains.

  • A–B · 549 Ų buried · 6 hydrogen bonds · protein-protein
  • A–P · 545 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 7K29 · Kelch domain of human KEAP1 bound to Nrf2 peptide, LDEETGEAL · the same entry in another collection · chain A against A, TM-score 1.00

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