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KEAP1 compound complex

Analyse KEAP1 compound complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7Q96
Type
protein
Length
570 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kelch-like ech-associated protein 1
UniProt
Q14145
Ligands
9P0, CL
Pockets
3 · best druggability 0.85

Structure

x-ray diffraction · 1 distinct chain · 0% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BKelch-like ech-associated protein 1protein2850% helix, 52% strandQ14145

Ligands and binding sites

  • 9P0 · 4-[(5S,8R)-5-(dimethylcarbamoyl)-8-[[(2S)-1-ethanoylpyrrolidin-2-yl]carbonylamino]-7,11-bis(oxidanylidene)-10-oxa-3-thia-6-azabicyclo[10.4.0]hexadeca-1(16),12,14-trien-16-yl]benzoic acid · ligand · chains A, B
  • CL · Chloride ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110080.850.861219P0, CL
21480.390.7330empty
3520.300.7616empty

Interfaces

1 interface between chains.

  • A–B · 620 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 7Q96 · Keap1 compound complex · the same entry in another collection · chain A against A, TM-score 1.00

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