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Crystal Structure of the adhesin domain of Epf from Streptococcus pyogenes in P212121

Analyse Crystal Structure of the adhesin domain of Epf from Streptococcus pyogenes in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4ES8
Type
protein
Length
599 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.58
Source
Streptococcus pyogenes
Molecule
Epf
Ligands
NA, K
Pockets
3 · best druggability 0.66

Structure

x-ray diffraction · resolution 1.58 · 2 distinct chains · 5% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEpfprotein3025% helix, 47% strand—
BEpfprotein2975% helix, 47% strand—

Ligands and binding sites

  • NA · Sodium ion · metal · chains A, B
  • K · Potassium ion · metal · chains B
  • ACT · Acetate ion · additive · 2 copies · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15360.660.7765NA
24940.620.7544empty
3930.370.7622empty

Interfaces

1 interface between chains.

  • A–B · 608 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 4ES8 · Crystal structure of the adhesin domain of epf from streptococcus pyogenes in P212121 · the same entry in another collection · chain A against A, TM-score 1.00

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