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MolNFT v1 · #190241 · protein

Cryo-EM structure of SARS-cov-2 C.1.2 S6P trimer in complex with neutralizing antibody vacw-209 (local refinement)

7WP2 · Vacw-209 light chain: “Cryo-EM structure of SARS-cov-2 C.1.2 S6P trimer in complex with neutralizing antibody vacw-209 (local…”. Electron microscopy, 1 ligand (NAG), 5 pockets (best druggability 0.45). MolNFT v1 #190241 on…

PDB
7WP2
Type
protein
Length
422 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Vacw-209 light chain; Vacw-209 heavy chain; Spike protein S1
UniProt
A0A5C2GQT9, P0DTC2
Ligands
NAG
Pockets
5 · best druggability 0.45

Structure

electron microscopy · 3 distinct chains · 2% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LVacw-209 light chainprotein1090% helix, 41% strandA0A5C2GQT9
HVacw-209 heavy chainprotein1312% helix, 40% strand—
FSpike protein S1protein1823% helix, 23% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.450.7528empty
21570.430.7528empty
3910.390.7716empty
4760.340.7516empty
5570.300.7513empty

Interfaces

3 interfaces between chains.

  • L–H · 887 Ų buried · 7 hydrogen bonds · protein-protein
  • H–F · 674 Ų buried · 1 hydrogen bond · protein-protein
  • L–F · 417 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 7WP2 · Cryo-EM structure of SARS-CoV-2 C.1.2 S6P trimer in complex with neutralizing antibody… · the same entry in another collection · chain L against L, TM-score 1.00

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