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Structural basis for shikimate-binding specificity of helicobacter pylori shikimate kinase

Analyse Structural basis for shikimate-binding specificity of helicobacter pylori… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ZUI
Type
protein
Length
158 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Shikimate kinase
EC
2.7.1.71
UniProt
P56073
Ligands
SKM, PO4
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 56% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AShikimate kinase (EC 2.7.1.71)protein15856% helix, 15% strandP56073

Ligands and binding sites

  • SKM · (3R,4S,5R)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid · ligand · chains A
  • PO4 · Phosphate ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1500.650.9517SKM
21030.410.7719PO4

Compared structures

  • 1ZUI · Structural Basis for Shikimate-binding Specificity of Helicobacter pylori Shikimate Kinase · the same entry in another collection · chain A against A, TM-score 1.00
  • P56073 · AlphaFold monomer V2.0 prediction for shikimate kinase (P56073) · a predicted model of the same protein · chain A against A, TM-score 0.95

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