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Salmonella typhi pltb homopentamer with neu-5NAC-9OAC-alpha-2-3-gal- beta-1-4-glcnac glycans

Analyse Salmonella typhi pltb homopentamer with neu-5NAC-9OAC-alpha-2-3-gal… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6TYN
Type
protein
Length
570 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pertussis like toxin subunit B
UniProt
Q8Z6A3
Ligands
5N6, NAG, GAL
Pockets
1 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 20% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, EPertussis like toxin subunit Bprotein11420% helix, 42% strandQ8Z6A3

Ligands and binding sites

  • 5N6 · 9-O-acetyl-5-acetamido-3,5-dideoxy-D-glycero-alpha-D-galacto-non-2-ulopyranosonic acid · ligand · 5 copies · chains A, C, D, E
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A, E
  • GAL · beta-D-galactopyranose · sugar · 5 copies · chains A, C, D, E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18010.670.7536empty

Interfaces

5 interfaces between chains.

  • C–D · 1081 Ų buried · 27 hydrogen bonds · protein-protein
  • A–B · 1053 Ų buried · 27 hydrogen bonds · protein-protein
  • B–E · 1051 Ų buried · 28 hydrogen bonds · protein-protein
  • D–E · 1045 Ų buried · 25 hydrogen bonds · protein-protein
  • A–C · 1017 Ų buried · 26 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • 6TYN · Salmonella Typhi PltB Homopentamer with Neu-5NAc-9OAc-alpha-2-3-Gal-beta-1-4-GlcNAc… · the same entry in another collection · chain A against A, TM-score 1.00

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