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Glycoprotein B from herpes simplex virus type 1, Y179S mutant, low-pH

Analyse Glycoprotein B from herpes simplex virus type 1, Y179S mutant, low-pH in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3NWD
Type
protein
Length
2,410 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Envelope glycoprotein B
UniProt
P06437
Ligands
MRY, NAG, CL
Pockets
20 · best druggability 0.60

Structure

x-ray diffraction · 4 distinct chains · 21% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BEnvelope glycoprotein Bprotein59720% helix, 36% strandP06437
AEnvelope glycoprotein Bprotein60621% helix, 33% strandP06437
CEnvelope glycoprotein Bprotein60120% helix, 32% strandP06437
DEnvelope glycoprotein Bprotein60621% helix, 33% strandP06437

Ligands and binding sites

  • MRY · Meso-erythritol · ligand · chains C
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 13 copies · chains B, D, A, C
  • CL · Chloride ion · ion · 2 copies · chains A, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12040.600.8131empty
21210.540.8228empty
31280.520.8126empty
42100.510.7626empty
51440.500.7926empty

Interfaces

1 interface between chains.

  • B–A · 541 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 20 disulfide, 11 glycan (disulfide, N-glycosylation).

Compared structures

  • 3NWD · Glycoprotein B from Herpes simplex virus type 1, Y179S mutant, low-pH · the same entry in another collection · chain B against B, TM-score 1.00

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