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Structural insights into thioether bond formation in the biosynthesis of sactipeptides

Analyse Structural insights into thioether bond formation in the biosynthesis of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5WGG
Type
protein
Length
451 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Radical SAM domain protein; Ctea
UniProt
A3DDW1, A3DDW2
Ligands
SF4, SAM, CA
Pockets
4 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARadical SAM domain proteinprotein44043% helix, 16% strandA3DDW1
BCteaprotein110% helix, 27% strandA3DDW2

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 3 copies · chains A, B
  • SAM · S-adenosylmethionine · ligand · chains A
  • CA · Calcium ion · metal · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19350.850.86101SF4, SAM
21190.470.7926empty
31160.370.7430empty
4540.370.8016empty

Interfaces

1 interface between chains.

  • A–B · 822 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 5WGG · Structural Insights into Thioether Bond Formation in the Biosynthesis of Sactipeptides · the same entry in another collection · chain A against A, TM-score 1.00

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