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GII.13/21 noroviruses recognize glycans with a terminal beta-galactose via an unconventional glycan binding site

Analyse GII.13/21 noroviruses recognize glycans with a terminal beta-galactose via an… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JYS
Type
protein
Length
1,232 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Human norovirus P protein
Ligands
THR, A2G, GAL, NAG
Pockets
15 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 6% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DHuman norovirus P proteinprotein3086% helix, 34% strand—

Ligands and binding sites

  • THR · Threonine · ligand · chains B
  • A2G · 2-acetamido-2-deoxy-alpha-D-galactopyranose · sugar · 4 copies · chains A, B, D, C
  • GAL · beta-D-galactopyranose · sugar · 4 copies · chains A, B, C, D
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11180.760.9631empty
22500.750.8932empty
33710.660.8043empty
43810.620.7754empty
51020.560.8523empty

Interfaces

4 interfaces between chains.

  • A–D · 2235 Ų buried · 31 hydrogen bonds · protein-protein
  • B–C · 410 Ų buried · 0 hydrogen bonds · protein-protein
  • B–D · 134 Ų buried · 4 hydrogen bonds · protein-protein
  • C–D · 33 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6JYS · GII.13/21 noroviruses recognize glycans with a terminal beta-galactose via an… · the same entry in another collection · chain B against B, TM-score 1.00

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