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Structural basis for immunization with post-fusion rsv F to elicit high neutralizing antibody titers

Analyse Structural basis for immunization with post-fusion rsv F to elicit high… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3RKI
Type
protein
Length
1,319 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fusion glycoprotein F0
UniProt
P03420
Ligands
NAG
Pockets
10 · best druggability 0.82

Structure

x-ray diffraction · 3 distinct chains · 39% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFusion glycoprotein F0protein44140% helix, 30% strandP03420
BFusion glycoprotein F0protein43940% helix, 30% strandP03420
CFusion glycoprotein F0protein43938% helix, 30% strandP03420

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 13 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110140.820.8396empty
29270.780.80117empty
32730.680.8326empty
41990.580.8143empty
5560.480.8519empty

Interfaces

3 interfaces between chains.

  • B–C · 6302 Ų buried · 66 hydrogen bonds · protein-protein
  • A–C · 6293 Ų buried · 69 hydrogen bonds · protein-protein
  • A–B · 6225 Ų buried · 61 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 21 disulfide, 7 glycan (disulfide, N-glycosylation).

Compared structures

  • 3RKI · Structural basis for immunization with post-fusion RSV F to elicit high neutralizing… · the same entry in another collection · chain A against A, TM-score 1.00

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