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Structure of khk in complex with compound 3

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

PDB
6W0W
Type
protein
Length
597 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ketohexokinase
EC
2.7.1.3
UniProt
P50053
Ligands
RZA, SO4
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKetohexokinase (EC 2.7.1.3)protein29637% helix, 25% strandP50053
BKetohexokinase (EC 2.7.1.3)protein30136% helix, 24% strandP50053

Ligands and binding sites

  • RZA · 6-[(3~{R},4~{S})-3,4-bis(oxidanyl)pyrrolidin-1-yl]-2-[(2~{S},3~{R})-2-methyl-3-oxidanyl-azetidin-1-yl]-4-(trifluoromethyl)pyridine-3-carbonitrile · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16630.780.8363RZA, SO4
29090.750.7892RZA, SO4
3900.440.7921empty
41540.440.7521empty

Interfaces

1 interface between chains.

  • A–B · 1661 Ų buried · 31 hydrogen bonds · protein-protein

Compared structures

  • 6W0W · Structure of KHK in complex with compound 3 · the same entry in another collection · chain A against A, TM-score 1.00
  • P50053 · AlphaFold monomer V2.0 prediction for ketohexokinase (P50053) · a predicted model of the same protein · chain A against A, TM-score 0.99

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