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Insights into substrate and metal binding from the crystal structure of cyanobacterial aldehyde deformylating oxygenase with substrate analogs bound

Analyse Insights into substrate and metal binding from the crystal structure of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PGI
Type
protein
Length
222 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aldehyde decarbonylase
EC
4.1.99.5
UniProt
Q7V6D4
Ligands
Y69, FE
Pockets
1 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 86% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAldehyde decarbonylase (EC 4.1.99.5)protein22286% helix, 0% strandQ7V6D4

Ligands and binding sites

  • Y69 · 11-[2-(2-ethoxyethoxy)ethoxy]undecanal · ligand · chains A
  • FE · Fe (III) ion · metal · 2 copies · chains A
  • EDO · 1,2-ethanediol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12330.800.9340Y69

Compared structures

  • 4PGI · Insights into Substrate and Metal Binding from the Crystal Structure of Cyanobacterial… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q7V6D4 · AlphaFold monomer V2.0 prediction for aldehyde decarbonylase (Q7V6D4) · a predicted model of the same protein · chain A against A, TM-score 0.99

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