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Crystal structure of the envelope glycoprotein prefusion complex of andes virus - mutant H953F

Analyse Crystal structure of the envelope glycoprotein prefusion complex of andes virus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6Y5F
Type
protein
Length
770 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Envelope POLYPROTEIN,ENVELOPE polyprotein
UniProt
A0A3Q8TA45
Ligands
NAG, BMA, MAN, PO4
Pockets
9 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEnvelope POLYPROTEIN,ENVELOPE polyproteinprotein35311% helix, 44% strandA0A3Q8TA45
BEnvelope POLYPROTEIN,ENVELOPE polyproteinprotein4175% helix, 54% strandA0A3Q8TA45

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains B
  • MAN · alpha-D-mannopyranose · sugar · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15050.650.7764empty
24030.650.7943empty
32620.610.8026empty
4520.530.8817empty
51370.490.7922empty

Interfaces

1 interface between chains.

  • A–B · 1581 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 20 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 6Y5F · Crystal structure of the envelope glycoprotein prefusion complex of Andes virus - Mutant… · the same entry in another collection · chain A against A, TM-score 1.00

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