MolNFT v1 · #179722 · protein
SARS-cov-2 D614G 3 rbd down spike protein trimer without the P986-P987 stabilizing mutations (S-gsas-D614G sub-class)
7KE4 · Spike glycoprotein: “SARS-cov-2 D614G 3 rbd down spike protein trimer without the P986-P987 stabilizing mutations (S-gsas-D614G…”. Electron microscopy, 1 ligand (NAG), 20 pockets (best druggability 0.82). MolNFT v1 #179722 on…
- PDB
- 7KE4
- Type
- protein
- Length
- 2,916 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 · 1 distinct chain · 23% helix, 33% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Spike glycoprotein | protein | 972 | 23% helix, 33% strand | P0DTC2 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 63 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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 960 | 0.82 | 0.84 | 101 | empty |
| 2 | 656 | 0.81 | 0.86 | 63 | empty |
| 3 | 617 | 0.81 | 0.86 | 74 | empty |
| 4 | 374 | 0.77 | 0.87 | 48 | empty |
| 5 | 357 | 0.76 | 0.87 | 45 | empty |
Interfaces
3 interfaces between chains.
- B–C · 5538 Ų buried · 49 hydrogen bonds · protein-protein
- A–B · 5409 Ų buried · 48 hydrogen bonds · protein-protein
- A–C · 5109 Ų buried · 46 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 48 glycan, 36 disulfide (N-glycosylation, disulfide).
Compared structures
- 7KE4 · SARS-CoV-2 D614G 3 RBD down Spike Protein Trimer without the P986-P987 stabilizing… · the same entry in another collection · chain A against A, 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 7KE4 · PDBe 7KE4 · UniProt P0DTC2
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