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MolNFT v1 · #181867 · protein

Cryo-EM structure of brazil (P.1) SARS-cov-2 spike glycoprotein variant in the prefusion state (1 rbd up)

7M8K: “Cryo-EM structure of brazil (P.1) SARS-cov-2 spike glycoprotein variant in the prefusion state (1 rbd up)”. Electron microscopy, 1 ligand (NAG), 20 pockets (best druggability 0.82). MolNFT v1 #181867 on GenesisL1: 3D structure…

PDB
7M8K
Type
protein
Length
3,084 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 0.82

Structure

electron microscopy · 3 distinct chains · 22% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein102524% helix, 31% strandP0DTC2
BSpike glycoproteinprotein103322% helix, 31% strandP0DTC2
CSpike glycoproteinprotein102621% helix, 32% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 51 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
16760.820.8672empty
27640.810.8484empty
35000.800.8752empty
47040.780.8375empty
56040.780.8444empty

Interfaces

3 interfaces between chains.

  • A–B · 4844 Ų buried · 40 hydrogen bonds · protein-protein
  • A–C · 4745 Ų buried · 38 hydrogen bonds · protein-protein
  • B–C · 4449 Ų buried · 28 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 40 glycan, 38 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7M8K · Cryo-EM structure of Brazil (P.1) SARS-CoV-2 spike glycoprotein variant in the prefusion… · the same entry in another collection · chain A against A, TM-score 1.00

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