GL1X · GenesisL1 explorer

MolNFT v1 · #4339 · protein

The substrate binding domain of dnak in complex with a substrate peptide, determined from type 1 selenomethionyl crystals

1DKX: “The substrate binding domain of dnak in complex with a substrate peptide, determined from type 1…”. X-ray diffraction, 3 pockets (best druggability 0.54). MolNFT v1 #4339 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
1DKX
Type
protein
Length
226 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Substrate binding domain of dnak; Substrate peptide (7 residues)
UniProt
P0A6Y8
Pockets
3 · best druggability 0.54

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASubstrate binding domain of dnakprotein21942% helix, 27% strandP0A6Y8
BSubstrate peptide (7 residues)protein70% helix, 29% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11120.540.8320empty
2850.340.7415empty
3580.280.7414empty

Interfaces

1 interface between chains.

  • A–B · 602 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 1DKX · The substrate binding domain of dnak in complex with a substrate peptide, determined from… · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A6Y8 · AlphaFold monomer V2.0 prediction for chaperone protein dnak (P0A6Y8) · a predicted model of the same protein · chain A against A, TM-score 0.48

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