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Crystal structure of PE8-PPE15 in complex with EspG5 from M. tuberculosis

Analyse Crystal structure of PE8-PPE15 in complex with EspG5 from M. tuberculosis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XFS
Type
protein
Length
526 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.9
Source
Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
Molecule
PE family protein PE8; PPE family protein PPE15; ESX-5 secretion-associated protein EspG5
UniProt
L7N667, P9WI31, O53943
Pockets
3 · best druggability 0.60

Structure

x-ray diffraction · resolution 2.9 · 3 distinct chains · 53% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APE family protein PE8protein7885% helix, 0% strandL7N667
BPPE family protein PPE15protein17377% helix, 0% strandP9WI31
CESX-5 secretion-associated protein EspG5protein27530% helix, 28% strandO53943

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11680.600.8332empty
21070.450.7824empty
31430.450.7619empty

Interfaces

2 interfaces between chains.

  • A–B · 2078 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 1345 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5XFS · Crystal structure of PE8-PPE15 in complex with ESPG5 from M. tuberculosis · the same entry in another collection · chain A against A, TM-score 1.00
  • O53943 · AlphaFold monomer V2.0 prediction for esx-5 secretion-associated protein ESPG5 (O53943) · a predicted model of the same protein · chain C against A, TM-score 0.99
  • P9WI31 · AlphaFold monomer V2.0 prediction for ppe family protein PPE15 (P9WI31) · a predicted model of the same protein · chain B against A, TM-score 0.97

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