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Superoxide reductase (neelaredoxin) from archaeoglobus fulgidus in the reduced form

Analyse Superoxide reductase (neelaredoxin) from archaeoglobus fulgidus in the reduced… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4BFF
Type
protein
Length
1,970 residues
Chains
16
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Superoxide reductase
EC
1.15.1.2
UniProt
O29903
Ligands
FE2
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 0% helix, 55% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, D, E, F, G, H, I, J, K, L, M, N, PSuperoxide reductase (EC 1.15.1.2)protein1230% helix, 54% strandO29903
C, OSuperoxide reductase (EC 1.15.1.2)protein1240% helix, 56% strandO29903

Ligands and binding sites

  • FE2 · Fe (II) ion · metal · 16 copies · chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P

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

Pockets

20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12380.850.9743empty
22500.850.9744empty
32520.850.9642empty
42540.840.9643empty
52310.840.9741empty

Interfaces

33 interfaces between chains.

  • M–N · 1220 Ų buried · 16 hydrogen bonds · protein-protein
  • E–F · 1212 Ų buried · 21 hydrogen bonds · protein-protein
  • K–L · 1200 Ų buried · 20 hydrogen bonds · protein-protein
  • G–H · 1193 Ų buried · 20 hydrogen bonds · protein-protein
  • A–B · 1184 Ų buried · 19 hydrogen bonds · protein-protein

Compared structures

  • 4BFF · Superoxide reductase (Neelaredoxin) from Archaeoglobus fulgidus in the reduced form · the same entry in another collection · chain P against P, TM-score 1.00

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