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Salmonella effector spvd - R161 variant

Analyse Salmonella effector spvd - R161 variant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LQ6
Type
protein
Length
184 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Virulence protein vsde
UniProt
P0A2N2
Ligands
NA
Pockets
2 · best druggability 0.31

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVirulence protein vsdeprotein18441% helix, 22% strandP0A2N2

Ligands and binding sites

  • NA · Sodium ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1790.310.7415empty
2550.300.7612empty

Compared structures

  • 5LQ6 · Salmonella effector SpvD - R161 variant · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A2N2 · AlphaFold monomer V2.0 prediction for virulence protein vsde (P0A2N2) · a predicted model of the same protein · chain A against A, TM-score 1.00

Analyse

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