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Myo-inositol kinase from thermococcus kodakarensis

Analyse Myo-inositol kinase from thermococcus kodakarensis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3W4S
Type
protein
Length
541 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CARBOHYDRATE/PYRIMIDINE kinase, pfkb family
UniProt
Q5JDA3
Ligands
IOD
Pockets
4 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACARBOHYDRATE/PYRIMIDINE kinase, pfkb familyprotein27331% helix, 32% strandQ5JDA3
BCARBOHYDRATE/PYRIMIDINE kinase, pfkb familyprotein26831% helix, 33% strandQ5JDA3

Ligands and binding sites

  • IOD · Iodide ion · ion · 30 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
15360.740.8255IOD
25130.730.8250IOD
3910.350.7422IOD
4780.290.7217IOD

Interfaces

1 interface between chains.

  • A–B · 688 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 3W4S · Myo-inositol kinase from Thermococcus kodakarensis · the same entry in another collection · chain A against A, TM-score 1.00

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