Research workbench
Crystal structure of the N501Y mutant receptor binding domain of SARS- cov-2 spike glycoprotein in complex with covox-222 and EY6A fabs
Analyse Crystal structure of the N501Y mutant receptor binding domain of SARS- cov-2… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7NX9
- Type
- protein
- Length
- 1,049 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- EY6A Fab heavy chain; EY6A Fab light chain; Spike protein S1; Covox-222 Fab heavy chain…
- UniProt
- P0DTC2
- Ligands
- NAG, SO4, CL
- Pockets
- 10 · best druggability 0.62
Structure
x-ray diffraction · 5 distinct chains · 8% helix, 48% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| H | EY6A Fab heavy chain | protein | 215 | 4% helix, 51% strand | — |
| L | EY6A Fab light chain | protein | 214 | 5% helix, 52% strand | — |
| E | Spike protein S1 | protein | 194 | 15% helix, 31% strand | P0DTC2 |
| A | Covox-222 Fab heavy chain | protein | 214 | 7% helix, 52% strand | — |
| B | Covox-222 Fab light chain | protein | 212 | 7% helix, 54% strand | — |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains E
- SO4 · Sulfate ion · ion · 10 copies · chains H, E, A, B
- CL · Chloride ion · ion · chains A
- GOL · Glycerol · additive · 3 copies · chains E, B, A
- PEG · Di(hydroxyethyl)ether · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 577 | 0.62 | 0.74 | 55 | PEG, CL |
| 2 | 422 | 0.56 | 0.73 | 53 | empty |
| 3 | 186 | 0.56 | 0.80 | 31 | GOL |
| 4 | 203 | 0.51 | 0.76 | 32 | empty |
| 5 | 174 | 0.48 | 0.76 | 24 | empty |
Interfaces
6 interfaces between chains.
- H–L · 1792 Ų buried · 10 hydrogen bonds · protein-protein
- A–B · 1678 Ų buried · 15 hydrogen bonds · protein-protein
- E–A · 720 Ų buried · 17 hydrogen bonds · protein-protein
- H–E · 642 Ų buried · 11 hydrogen bonds · protein-protein
- L–E · 437 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 12 disulfide, 1 glycan (disulfide, N-glycosylation).
Compared structures
- 7NX9 · Crystal structure of the N501Y mutant receptor binding domain of SARS-CoV-2 Spike… · the same entry in another collection · chain H against H, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P0DTC2
- Elsewhere: RCSB PDB 7NX9 · PDBe 7NX9 · UniProt P0DTC2
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.