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Crystal structure of E. COLI bacterioferritin (bfr) soaked in phosphate with an alternative conformation of the unoccupied ferroxidase centre (apo-bfr II).

Analyse Crystal structure of E. COLI bacterioferritin (bfr) soaked in phosphate with an… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3E1L
Type
protein
Length
1,896 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bacterioferritin
UniProt
P0ABD3
Ligands
HEM, SO4
Pockets
20 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 77% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LBacterioferritinprotein15877% helix, 0% strandP0ABD3

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 6 copies · chains A, B, C, D, E, F, G, H, I, J, K, L
  • SO4 · Sulfate ion · ion · 16 copies · chains A, J, B, G, C, H, D, E, F, L, K, I

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

Pockets

20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13760.730.8530empty
21820.720.8832HEM
32070.700.8634HEM
41860.700.8730HEM
51890.690.8630HEM

Interfaces

24 interfaces between chains.

  • G–H · 966 Ų buried · 12 hydrogen bonds · protein-protein
  • K–L · 966 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 965 Ų buried · 12 hydrogen bonds · protein-protein
  • E–F · 965 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 964 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 3E1L · Crystal structure of E. coli Bacterioferritin (BFR) soaked in phosphate with an… · the same entry in another collection · chain J against J, TM-score 1.00

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