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Crystal structure of cyanobacterial aldehyde-deformylating oxygenase bound with fatty acid

Analyse Crystal structure of cyanobacterial aldehyde-deformylating oxygenase bound with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RC8
Type
protein
Length
444 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aldehyde decarbonylase
EC
4.1.99.5
UniProt
Q54764
Ligands
STE, FE
Pockets
2 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 87% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAldehyde decarbonylase (EC 4.1.99.5)protein22287% helix, 0% strandQ54764

Ligands and binding sites

  • STE · Stearic acid · ligand · chains A
  • FE · Fe (III) ion · metal · 2 copies · chains A

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

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11560.820.9730STE
23090.760.8760empty

Interfaces

1 interface between chains.

  • A–B · 1091 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 4RC8 · Crystal structure of cyanobacterial aldehyde-deformylating oxygenase bound with fatty acid · the same entry in another collection · chain A against A, TM-score 1.00
  • Q54764 · AlphaFold monomer V2.0 prediction for aldehyde decarbonylase (Q54764) · a predicted model of the same protein · chain A against A, TM-score 0.99

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