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Crystal structure of mouse TLR9 in complex with inhibitory DNA4084 (form 2)

Analyse Crystal structure of mouse TLR9 in complex with inhibitory DNA4084 (form 2) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WPH
Type
protein + DNA
Length
737 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Toll-like receptor 9; DNA (5'-D(*CP*CP*TP*GP*GP*AP*TP*GP*GP*GP*AP*A)-3')
UniProt
Q9EQU3
Ligands
NAG, SO4
Pockets
5 · best druggability 0.60

Structure

x-ray diffraction · 2 distinct chains · 11% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AToll-like receptor 9protein72511% helix, 16% strandQ9EQU3
BDNA (5'-D(*CP*CP*TP*GP*GP*AP*TP*GP*GP*GP*AP*A)-3')dna12——

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1780.600.8914SO4
2710.580.8918empty
31220.500.8024empty
4890.340.7418empty
5520.310.7612empty

Interfaces

1 interface between chains.

  • A–B · 1253 Ų buried · 34 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 8 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 3WPH · Crystal structure of mouse TLR9 in complex with inhibitory DNA4084 (form 2) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9EQU3 · AlphaFold monomer V2.0 prediction for toll-like receptor 9 (Q9EQU3) · a predicted model of the same protein · chain A against A, TM-score 0.99

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