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Glutamate 5-kinase from escherichia COLI complexed with glutamyl-5-phosphate and pyroglutamic acid

Analyse Glutamate 5-kinase from escherichia COLI complexed with glutamyl-5-phosphate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2J5V
Type
protein
Length
648 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutamate 5-kinase
EC
2.7.2.11
UniProt
P0A7B5
Ligands
PCA, RGP, MG, SO4
Pockets
6 · best druggability 0.60

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutamate 5-kinase (EC 2.7.2.11)protein32345% helix, 20% strandP0A7B5
BGlutamate 5-kinase (EC 2.7.2.11)protein32543% helix, 22% strandP0A7B5

Ligands and binding sites

  • PCA · Pyroglutamic acid · ligand · 2 copies · chains A, B
  • RGP · Gamma-glutamyl phosphate · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · chains A
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14050.600.7639empty
22050.530.7724empty
31730.500.7720empty
41520.420.7433MG, PCA, RGP, SO4
51340.410.7527PCA, RGP, SO4

Interfaces

1 interface between chains.

  • A–B · 2291 Ų buried · 45 hydrogen bonds · protein-protein

Compared structures

  • 2J5V · Glutamate 5-kinase from escherichia COLI complexed with glutamyl-5-phosphate and… · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A7B5 · AlphaFold monomer V2.0 prediction for glutamate 5-kinase (P0A7B5) · a predicted model of the same protein · chain A against A, TM-score 1.00

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