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Crystal structure of the superantigen smez-2 (zinc bound) from streptococcus pyogenes

Analyse Crystal structure of the superantigen smez-2 (zinc bound) from streptococcus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1EU3
Type
protein
Length
418 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Superantigen smez-2
UniProt
Q9RQQ5
Ligands
ZN, K, PO4
Pockets
4 · best druggability 0.55

Structure

x-ray diffraction · 2 distinct chains · 19% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASuperantigen smez-2protein21020% helix, 41% strandQ9RQQ5
BSuperantigen smez-2protein20818% helix, 41% strandQ9RQQ5

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • K · Potassium ion · metal · chains A
  • PO4 · Phosphate ion · ion · 3 copies · chains B

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
11620.550.8123empty
21960.480.7634empty
3560.330.7819empty
4580.290.7415empty

Interfaces

1 interface between chains.

  • A–B · 563 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 1EU3 · Crystal structure of the superantigen smez-2 (zinc bound) from streptococcus pyogenes · the same entry in another collection · chain A against A, TM-score 1.00

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