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Structure of FTMOX1 apo with metal iron

Analyse Structure of FTMOX1 apo with metal iron in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Y5T
Type
protein
Length
574 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Verruculogen synthase
EC
1.14.11.38
UniProt
Q4WAW9
Ligands
FE2, CO, SO4
Pockets
6 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 26% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVerruculogen synthase (EC 1.14.11.38)protein28926% helix, 23% strandQ4WAW9
BVerruculogen synthase (EC 1.14.11.38)protein28526% helix, 24% strandQ4WAW9

Ligands and binding sites

  • FE2 · Fe (II) ion · metal · 2 copies · chains A, B
  • CO · Cobalt (II) ion · metal · chains B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1990.770.9823empty
25070.750.8351FE2, MES
35210.740.8250FE2, SO4
42350.560.7822empty
52190.520.7622empty

Interfaces

1 interface between chains.

  • A–B · 2556 Ų buried · 49 hydrogen bonds · protein-protein

Compared structures

  • 4Y5T · Structure of FtmOx1 apo with metal Iron · the same entry in another collection · chain A against A, TM-score 1.00
  • Q4WAW9 · AlphaFold monomer V2.0 prediction for verruculogen synthase (Q4WAW9) · a predicted model of the same protein · chain B against A, TM-score 1.00

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