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MolNFT v1 · #170389 · protein

Crystal structure of the envelope glycoprotein complex of andes virus in a near postfusion conformation

6Y5W · Envelope POLYPROTEIN,ENVELOPE polyprotein: “Crystal structure of the envelope glycoprotein complex of andes virus in a near postfusion conformation”. X-ray diffraction, 3 ligands (NAG, BMA, MAN), 5 pockets (best druggability 0.80).…

PDB
6Y5W
Type
protein
Length
754 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
Pockets
5 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEnvelope POLYPROTEIN,ENVELOPE polyproteinprotein34911% helix, 44% strandA0A3Q8TA45
BEnvelope POLYPROTEIN,ENVELOPE polyproteinprotein4055% helix, 57% strandA0A3Q8TA45

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 3 copies · chains B, A
  • MAN · alpha-D-mannopyranose · sugar · 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, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110670.800.81107empty
21850.590.8138empty
32080.550.7933empty
41900.520.7830empty
52750.500.7438empty

Interfaces

1 interface between chains.

  • A–B · 1773 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 19 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 6Y5W · Crystal structure of the envelope glycoprotein complex of Andes virus in a near… · the same entry in another collection · chain A against A, TM-score 1.00

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