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Delta (B.1.617.2) SARS-cov-2 variant spike protein (S-gsas-delta) in the 1-rbd-up conformation; subclassification D15 state

Analyse Delta (B.1.617.2) SARS-cov-2 variant spike protein (S-gsas-delta) in the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TPC
Type
protein
Length
2,983 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 · 23% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein100524% helix, 33% strandP0DTC2
BSpike glycoproteinprotein97523% helix, 31% strandP0DTC2
CSpike glycoproteinprotein100324% helix, 33% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 58 copies · chains A, C, B

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
17280.850.8871empty
28640.820.8487empty
36820.810.8567empty
46440.800.8570empty
52870.800.9153empty

Interfaces

3 interfaces between chains.

  • A–B · 4609 Ų buried · 45 hydrogen bonds · protein-protein
  • A–C · 4528 Ų buried · 43 hydrogen bonds · protein-protein
  • B–C · 4043 Ų buried · 42 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 46 glycan, 37 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7TPC · Delta (B.1.617.2) SARS-CoV-2 variant spike protein (S-GSAS-Delta) in the 1-RBD-up… · the same entry in another collection · chain A against A, TM-score 1.00

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