GL1X · GenesisL1 explorer

Research workbench

SARS-cov-2 S/S2M11/S2M28 local refinement

Analyse SARS-cov-2 S/S2M11/S2M28 local refinement in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7LY0
Type
protein
Length
354 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein; S2M28 Fab light chain variable region; S2M28 Fab heavy chain variable…
UniProt
P0DTC2
Ligands
NAG, MAN, FUC
Pockets
2 · best druggability 0.40

Structure

electron microscopy · 3 distinct chains · 5% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein1312% helix, 50% strandP0DTC2
LS2M28 Fab light chain variable regionprotein1067% helix, 44% strand—
HS2M28 Fab heavy chain variable regionprotein1178% helix, 50% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, H
  • MAN · alpha-D-mannopyranose · sugar
  • FUC · alpha-L-fucopyranose · sugar

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1750.400.7818empty
2770.310.7317empty

Interfaces

3 interfaces between chains.

  • L–H · 833 Ų buried · 10 hydrogen bonds · protein-protein
  • A–H · 644 Ų buried · 8 hydrogen bonds · protein-protein
  • A–L · 592 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 7LY0 · SARS-CoV-2 S/S2M11/S2M28 Local Refinement · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.