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Structure of the soluble AhlB of the tripartite alpha-pore forming toxin, AHL, from Aeromonas hydrophila.

Analyse Structure of the soluble AhlB of the tripartite alpha-pore forming toxin, AHL… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6GRK
Type
protein
Length
1,055 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.33
Source
Aeromonas hydrophila
Molecule
AhlB
UniProt
A0A081US78
Pockets
15 · best druggability 0.72

Structure

x-ray diffraction · resolution 2.33 · 2 distinct chains · 77% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, IAhlBprotein35476% helix, 4% strandA0A081US78
BAhlBprotein34778% helix, 4% strandA0A081US78

Pockets

15 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19530.720.7694empty
2670.610.9118empty
3670.600.9021empty
4610.580.9019empty
51400.490.7826empty

Interfaces

3 interfaces between chains.

  • A–B · 907 Ų buried · 2 hydrogen bonds · protein-protein
  • A–I · 600 Ų buried · 9 hydrogen bonds · protein-protein
  • I–B · 78 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6GRK · Structure of the soluble ahlb of the tripartite alpha-pore forming toxin, ahl, from… · the same entry in another collection · chain A against A, TM-score 1.00

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