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MolNFT v1 · #183318 · protein

SARS-cov-2 spike rbd (dimer) in complex with two FU2 nanobodies

7NLL · Surface glycoprotein: “SARS-cov-2 spike rbd (dimer) in complex with two FU2 nanobodies”. Electron microscopy, 1 ligand (RTV), 6 pockets (best druggability 0.78). MolNFT v1 #183318 on GenesisL1: 3D structure, binding sites and…

PDB
7NLL
Type
protein
Length
656 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Surface glycoprotein; Nanobody FU2
UniProt
A0A6H1XM27
Ligands
RTV
Pockets
6 · best druggability 0.78

Structure

electron microscopy · 4 distinct chains · 11% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BSurface glycoproteinprotein19615% helix, 26% strandA0A6H1XM27
DSurface glycoproteinprotein19515% helix, 26% strandA0A6H1XM27
ANanobody FU2protein1335% helix, 45% strand—
CNanobody FU2protein1325% helix, 45% strand—

Ligands and binding sites

  • RTV · 2-(acetylamino)-1,5-anhydro-2-deoxy-D-mannitol · ligand · 2 copies · chains B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18730.780.8194empty
21060.370.7424empty
3760.360.7621empty
4790.360.7621empty
5850.330.7419empty

Interfaces

5 interfaces between chains.

  • B–C · 772 Ų buried · 13 hydrogen bonds · protein-protein
  • D–A · 766 Ų buried · 16 hydrogen bonds · protein-protein
  • D–C · 550 Ų buried · 4 hydrogen bonds · protein-protein
  • B–A · 548 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 13 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • 7NLL · SARS-CoV-2 Spike RBD (dimer) in complex with two Fu2 nanobodies · the same entry in another collection · chain B against B, TM-score 1.00

Analyse

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