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Structure of the cytosolic domain of E. COLI feob, GPPCH2P-bound form

Analyse Structure of the cytosolic domain of E. COLI feob, GPPCH2P-bound form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3I92
Type
protein
Length
778 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ferrous iron transport protein B
UniProt
P33650
Ligands
GCP, MG
Pockets
6 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 49% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFerrous iron transport protein Bprotein25747% helix, 18% strandP33650
BFerrous iron transport protein Bprotein26049% helix, 17% strandP33650
CFerrous iron transport protein Bprotein26149% helix, 15% strandP33650

Ligands and binding sites

  • GCP · Phosphomethylphosphonic acid guanylate ester · ligand · 3 copies · chains A, B, C
  • MG · Magnesium ion · metal · 3 copies · chains A, B, C

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18580.800.8261empty
28800.780.8098empty
31550.520.7922empty
41720.470.7631empty
5560.430.8217empty

Interfaces

3 interfaces between chains.

  • A–C · 712 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 654 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 191 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 3I92 · Structure of the cytosolic domain of E. coli FeoB, GppCH2p-bound form · the same entry in another collection · chain A against A, TM-score 1.00
  • P33650 · AlphaFold monomer V2.0 prediction for FE(2+) transporter feob (P33650) · a predicted model of the same protein · chain B against A, TM-score 0.99

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