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MolNFT v1 · #171756 · protein

Association of two complexes of largely structurally disordered spike ectodomain with bound EY6A Fab

6ZFO · Spike protein S1: “Association of two complexes of largely structurally disordered spike ectodomain with bound EY6A Fab”. Electron microscopy, 1 ligand (NAG), 13 pockets (best druggability 0.75). MolNFT v1 #171756 on GenesisL1: 3D…

PDB
6ZFO
Type
protein
Length
1,252 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike protein S1; EY6A heavy chain; EY6A light chain
UniProt
P0DTC2
Ligands
NAG
Pockets
13 · best druggability 0.75

Structure

electron microscopy · 3 distinct chains · 7% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
E, ASpike protein S1protein19411% helix, 29% strandP0DTC2
H, BEY6A heavy chainprotein2183% helix, 49% strand—
L, CEY6A light chainprotein2147% helix, 55% strand—

Ligands and binding sites

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

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

Pockets

13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17080.750.8071empty
28170.720.7756empty
34140.580.7554empty
43120.580.7753empty
54260.580.7450empty

Interfaces

7 interfaces between chains.

  • B–C · 1983 Ų buried · 10 hydrogen bonds · protein-protein
  • H–L · 1981 Ų buried · 10 hydrogen bonds · protein-protein
  • E–H · 624 Ų buried · 7 hydrogen bonds · protein-protein
  • E–A · 618 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 606 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 6ZFO · Association of two complexes of largely structurally disordered Spike ectodomain with… · the same entry in another collection · chain E against E, TM-score 1.00

Analyse

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