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Crystal structure of vvplpa G389N from vibrio vulnificus

Analyse Crystal structure of vvplpa G389N from vibrio vulnificus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JL2
Type
protein
Length
1,178 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thermolabile hemolysin
UniProt
A0A2S3SYP4
Ligands
1PS
Pockets
12 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 38% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThermolabile hemolysinprotein40139% helix, 18% strandA0A2S3SYP4
BThermolabile hemolysinprotein39138% helix, 19% strandA0A2S3SYP4
CThermolabile hemolysinprotein38638% helix, 19% strandA0A2S3SYP4

Ligands and binding sites

  • 1PS · 3-pyridinium-1-ylpropane-1-sulfonate · ligand · 7 copies · chains A, B, C
  • P6G · Hexaethylene glycol · additive · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.810.9633P6G
25910.790.85611PS
35860.780.84691PS
46030.780.84631PS
52140.770.9144P6G

Interfaces

3 interfaces between chains.

  • B–C · 786 Ų buried · 1 hydrogen bond · protein-protein
  • A–B · 649 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 552 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 6JL2 · Crystal structure of VvPlpA G389N from Vibrio vulnificus · the same entry in another collection · chain A against A, TM-score 1.00

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