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La crosse virus envelope glycoprotein gc W1066H mutant fusion domains in postfusion conformation

Analyse La crosse virus envelope glycoprotein gc W1066H mutant fusion domains in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7A57
Type
protein
Length
1,322 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Envelopment polyprotein
UniProt
Q8JPR1
Ligands
NAG, FUC
Pockets
16 · best druggability 0.88

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEnvelopment polyproteinprotein4375% helix, 53% strandQ8JPR1
BEnvelopment polyproteinprotein4496% helix, 51% strandQ8JPR1
CEnvelopment polyproteinprotein4365% helix, 53% strandQ8JPR1

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, C, B
  • FUC · alpha-L-fucopyranose · sugar · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110160.880.9098empty
24670.810.8961empty
3680.740.9915empty
49330.720.77101empty
51510.700.8925empty

Interfaces

3 interfaces between chains.

  • A–C · 3082 Ų buried · 40 hydrogen bonds · protein-protein
  • B–C · 3039 Ų buried · 42 hydrogen bonds · protein-protein
  • A–B · 3003 Ų buried · 38 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 30 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 7A57 · La Crosse Virus Envelope Glycoprotein Gc W1066H Mutant Fusion Domains in Postfusion… · the same entry in another collection · chain A against A, TM-score 1.00

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