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Structure of the salmonella virulence effector sptp in complex with its secretion chaperone sicp

Analyse Structure of the salmonella virulence effector sptp in complex with its… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1JYO
Type
protein
Length
726 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sicp; Protein tyrosine phosphatase sptp
UniProt
O85300, P74873
Pockets
9 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 48% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DSicpprotein13045% helix, 28% strandO85300
EProtein tyrosine phosphatase sptpprotein10251% helix, 12% strandP74873
FProtein tyrosine phosphatase sptpprotein10448% helix, 10% strandP74873

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12850.610.7937empty
22430.600.8032empty
32020.560.7939empty
42020.490.7635empty
51160.450.7824empty

Interfaces

9 interfaces between chains.

  • D–E · 1627 Ų buried · 18 hydrogen bonds · protein-protein
  • C–F · 1616 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 1180 Ų buried · 15 hydrogen bonds · protein-protein
  • B–D · 1170 Ų buried · 15 hydrogen bonds · protein-protein
  • A–F · 1120 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 1JYO · Structure of the Salmonella Virulence Effector SptP in Complex with its Secretion… · the same entry in another collection · chain F against F, TM-score 1.00
  • P74873 · AlphaFold monomer V2.0 prediction for secreted effector protein sptp (P74873) · a predicted model of the same protein · chain F against A, TM-score 0.41

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