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Glucosamine kinase (crystal form B)

Analyse Glucosamine kinase (crystal form B) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6HWK
Type
protein
Length
1,639 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glucosamine kinase
UniProt
A0A1H7TQR5
Ligands
MG, CL
Pockets
17 · best druggability 0.73

Structure

x-ray diffraction · 4 distinct chains · 49% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlucosamine kinaseprotein41249% helix, 18% strandA0A1H7TQR5
BGlucosamine kinaseprotein40350% helix, 17% strandA0A1H7TQR5
CGlucosamine kinaseprotein40849% helix, 18% strandA0A1H7TQR5
DGlucosamine kinaseprotein41649% helix, 18% strandA0A1H7TQR5

Ligands and binding sites

  • MG · Magnesium ion · metal · 3 copies · chains A, C, D
  • CL · Chloride ion · ion · 4 copies · chains A, B, C, D

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

Pockets

17 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18180.730.7776empty
25660.700.7967empty
310370.690.7490empty
44920.660.7849empty
53150.650.8149empty

Interfaces

4 interfaces between chains.

  • A–D · 407 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 392 Ų buried · 8 hydrogen bonds · protein-protein
  • C–D · 169 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 12 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6HWK · Glucosamine kinase (crystal form B) · the same entry in another collection · chain A against A, TM-score 1.00

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