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MolNFT v1 · #188176 · protein

Cryo-EM structure of SARS-cov-2 kappa (B.1.617.1) Q484I spike protein (focused refinement of rbd)

7TF1 · Spike glycoprotein: “Cryo-EM structure of SARS-cov-2 kappa (B.1.617.1) Q484I spike protein (focused refinement of rbd)”. Electron microscopy, 1 ligand (NAG), 20 pockets (best druggability 0.75). MolNFT v1 #188176 on GenesisL1: 3D…

PDB
7TF1
Type
protein
Length
1,608 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.75

Structure

electron microscopy · 1 distinct chain · 10% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FSpike glycoproteinprotein26810% helix, 34% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 12 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1930.750.9622empty
21060.750.9522empty
3940.730.9423empty
45630.700.7950empty
54070.650.7833empty

Interfaces

6 interfaces between chains.

  • B–F · 757 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 741 Ų buried · 10 hydrogen bonds · protein-protein
  • C–E · 719 Ų buried · 10 hydrogen bonds · protein-protein
  • C–F · 584 Ų buried · 10 hydrogen bonds · protein-protein
  • A–E · 566 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 disulfide, 12 glycan (disulfide, N-glycosylation).

Compared structures

  • 7TF1 · Cryo-EM structure of SARS-CoV-2 Kappa (B.1.617.1) Q484I spike protein (focused refinement… · the same entry in another collection · chain E against E, TM-score 1.00

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