GL1X · GenesisL1 explorer

MolNFT v1 · #64923 · protein

Crystal structure of E. COLI W35F bfr mutant

3GHQ · Bacterioferritin: “Crystal structure of E. COLI W35F bfr mutant”. X-ray diffraction, 3 ligands (HEM, FE, SO4), 20 pockets (best druggability 0.73). MolNFT v1 #64923 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
3GHQ
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, FE, SO4
Pockets
20 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 78% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LBacterioferritinprotein15878% 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
  • FE · Fe (III) ion · metal · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L
  • SO4 · Sulfate ion · ion · 21 copies · chains A, J, B, C, H, D, E, F, L, I, K, G

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

Pockets

20 pockets found on a 1 Å grid, 17 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13500.730.8531empty
21970.730.8930HEM
32070.700.8629HEM
41920.700.8730HEM
52110.700.8636HEM

Interfaces

24 interfaces between chains.

  • G–H · 950 Ų buried · 14 hydrogen bonds · protein-protein
  • K–L · 942 Ų buried · 14 hydrogen bonds · protein-protein
  • E–F · 942 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 942 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 938 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 3GHQ · Crystal Structure of E. coli W35F BFR mutant · the same entry in another collection · chain L against L, TM-score 1.00

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