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Mycobacterium tuberculosis bacterioferritin, bfra

Analyse Mycobacterium tuberculosis bacterioferritin, bfra in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3UOI
Type
protein
Length
7,632 residues
Chains
48
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bacterioferritin
EC
1.16.3.1
UniProt
P63697
Ligands
HEM
Pockets
20 · best druggability 0.80

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, X, a, b, c, d, e, f, g, h, i, j, k, l, m, n, o, p, q, r, s, t, u, v, w, xBacterioferritin (EC 1.16.3.1)protein15977% helix, 0% strandP63697

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 24 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, 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
111830.800.82100empty
22170.760.9029HEM
32220.750.8928HEM
41960.740.9027HEM
52340.740.8829HEM

Interfaces

147 interfaces between chains.

  • o–p · 998 Ų buried · 18 hydrogen bonds · protein-protein
  • a–b · 990 Ų buried · 17 hydrogen bonds · protein-protein
  • Q–R · 984 Ų buried · 16 hydrogen bonds · protein-protein
  • q–r · 982 Ų buried · 16 hydrogen bonds · protein-protein
  • U–V · 981 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 3UOI · Mycobacterium tuberculosis bacterioferritin, BfrA · the same entry in another collection · chain P against P, TM-score 1.00

Analyse

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