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Crystal structure of sphingomonas sp. A1 peroxidase efeb responsible for import of iron

Analyse Crystal structure of sphingomonas sp. A1 peroxidase efeb responsible for import… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JBN
Type
protein
Length
781 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peroxidase efeb
Ligands
HEM, OXY
Pockets
9 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeroxidase efebprotein39127% helix, 23% strand—
BPeroxidase efebprotein39027% helix, 23% strand—

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • OXY · Oxygen molecule · ion · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 24 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 5 copies · chains A, B
  • PGE · Triethylene glycol · additive · 3 copies · chains B, A

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

Pockets

9 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13040.840.9444HEM, OXY
23080.830.9346HEM, OXY
34260.700.8158PEG, EDO, PGE
44110.660.7960EDO, PEG
51270.450.7727EDO

Interfaces

1 interface between chains.

  • A–B · 3735 Ų buried · 51 hydrogen bonds · protein-protein

Compared structures

  • 6JBN · Crystal structure of Sphingomonas sp. A1 peroxidase EfeB responsible for import of iron · the same entry in another collection · chain A against A, TM-score 1.00

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