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Structure of the catalytic domain of the salmonella virulence factor ssei

Analyse Structure of the catalytic domain of the salmonella virulence factor ssei in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4G2B
Type
protein
Length
337 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Secreted effector protein ssei
UniProt
Q8ZQ79
Pockets
2 · best druggability 0.48

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASecreted effector protein sseiprotein16936% helix, 24% strandQ8ZQ79
BSecreted effector protein sseiprotein16835% helix, 24% strandQ8ZQ79

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11230.480.7924empty
2900.460.8123empty

Interfaces

1 interface between chains.

  • A–B · 902 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 4G2B · Structure of the Catalytic Domain of the Salmonella Virulence Factor SseI · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8ZQ79 · AlphaFold monomer V2.0 prediction for secreted effector protein ssei (Q8ZQ79) · a predicted model of the same protein · chain A against A, TM-score 0.98

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