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Iron storage and electron transport

Analyse Iron storage and electron transport in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1BFR
Type
protein
Length
3,792 residues
Chains
24
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bacterioferritin
UniProt
P0ABD3
Ligands
HEM, MN
Pockets
20 · best druggability 0.76

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, L, M, N, O, P, Q, R, S, T, U, V, W, XBacterioferritinprotein15877% helix, 0% strandP0ABD3

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X
  • MN · Manganese (II) ion · metal · 48 copies · chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12540.760.8932HEM
22550.750.8834HEM
32600.750.8834HEM
42530.750.8832HEM
52520.740.8830HEM

Interfaces

72 interfaces between chains.

  • Q–R · 983 Ų buried · 15 hydrogen bonds · protein-protein
  • E–F · 982 Ų buried · 15 hydrogen bonds · protein-protein
  • G–H · 981 Ų buried · 15 hydrogen bonds · protein-protein
  • M–N · 980 Ų buried · 15 hydrogen bonds · protein-protein
  • O–P · 979 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 1BFR · Iron storage and electron transport · the same entry in another collection · chain H against H, TM-score 1.00

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