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Cryo-EM structure of mature spondweni virus

Analyse Cryo-EM structure of mature spondweni virus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ZQV
Type
protein
Length
1,734 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Genome polyprotein
UniProt
C8XPB6, A0A2L1GGB4
Ligands
3PE, NAG, FUC
Pockets
20 · best druggability 0.88

Structure

electron microscopy · 2 distinct chains · 26% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, EGenome polyproteinprotein50421% helix, 39% strandC8XPB6
B, D, FGenome polyproteinprotein7458% helix, 0% strandA0A2L1GGB4

Ligands and binding sites

  • 3PE · 1,2-diacyl-sn-glycero-3-phosphoethanolamine · ligand · 3 copies · chains A, B, C, D, E, F
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, C, E
  • FUC · alpha-L-fucopyranose · sugar · 3 copies · chains A, C, E

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

Pockets

20 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110920.880.89119empty
211550.730.77963PE
36240.680.7771empty
44210.650.7964empty
51100.610.8719empty

Interfaces

9 interfaces between chains.

  • A–B · 1778 Ų buried · 17 hydrogen bonds · protein-protein
  • E–F · 1771 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 1750 Ų buried · 17 hydrogen bonds · protein-protein
  • C–E · 1581 Ų buried · 14 hydrogen bonds · protein-protein
  • D–F · 1147 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 6ZQV · Cryo-EM structure of mature Spondweni virus · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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