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South african (B.1.351) SARS-cov-2 spike protein variant (S-gsas- B.1.351) in the 1-rbd-up conformation

Analyse South african (B.1.351) SARS-cov-2 spike protein variant (S-gsas- B.1.351) in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7LYP
Type
protein
Length
2,985 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 3 distinct chains · 24% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein99623% helix, 34% strandP0DTC2
BSpike glycoproteinprotein99624% helix, 32% strandP0DTC2
CSpike glycoproteinprotein99324% helix, 33% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 28 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19070.850.8796empty
28140.840.87102empty
38650.840.8694empty
45600.820.8860empty
54500.780.8749empty

Interfaces

3 interfaces between chains.

  • A–C · 5098 Ų buried · 51 hydrogen bonds · protein-protein
  • A–B · 5027 Ų buried · 43 hydrogen bonds · protein-protein
  • B–C · 4480 Ų buried · 40 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 37 disulfide, 28 glycan (disulfide, N-glycosylation).

Compared structures

  • 7LYP · South African (B.1.351) SARS-CoV-2 spike protein variant (S-GSAS-B.1.351) in the 1-RBD-up… · the same entry in another collection · chain A against A, TM-score 1.00

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