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Crystal structure of W133F variant E. COLI bacterioferritn with iron.

Analyse Crystal structure of W133F variant E. COLI bacterioferritn with iron. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3E1Q
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, FE2, 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
  • FE2 · Fe (II) ion · metal · 24 copies · chains A, B, C, D, E, F, G, H, I, J, K, L
  • SO4 · Sulfate ion · ion · 16 copies · chains A, J, B, C, H, D, E, F, I, K, G, L

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
13260.730.8530empty
22180.720.8731HEM
32050.700.8630HEM
42120.700.8632HEM
52170.700.8631HEM

Interfaces

24 interfaces between chains.

  • G–H · 946 Ų buried · 14 hydrogen bonds · protein-protein
  • E–F · 942 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 939 Ų buried · 14 hydrogen bonds · protein-protein
  • I–J · 939 Ų buried · 14 hydrogen bonds · protein-protein
  • K–L · 937 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 3E1Q · Crystal structure of W133F variant E. coli Bacterioferritn with iron. · the same entry in another collection · chain L against L, TM-score 1.00

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