Research workbench
Human rhinovirus 16 coat protein in complex with antiviral compound VP65099
Analyse Human rhinovirus 16 coat protein in complex with antiviral compound VP65099 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1QJY
- Type
- protein
- Length
- 804 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein VP1; Protein VP2; Protein VP3; Protein VP4
- UniProt
- Q82122
- Ligands
- W03, MYR, ZN
- Pockets
- 12 · best druggability 0.76
Structure
x-ray diffraction · 4 distinct chains · 12% helix, 33% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| 1 | Protein VP1 | protein | 285 | 15% helix, 31% strand | Q82122 |
| 2 | Protein VP2 | protein | 252 | 12% helix, 37% strand | Q82122 |
| 3 | Protein VP3 | protein | 238 | 9% helix, 31% strand | Q82122 |
| 4 | Protein VP4 | protein | 29 | 10% helix, 28% strand | Q82122 |
Ligands and binding sites
- W03 · 2,6-dimethyl-1-(3-[3-methyl-5-isoxazolyl]-propanyl)-4-[2-methyl-4-isoxazolyl]-phenol · ligand · chains 1, 3
- MYR · Myristic acid · ligand · chains 4
- ZN · Zinc ion · metal · chains 1
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 420 | 0.76 | 0.85 | 68 | W03 |
| 2 | 228 | 0.55 | 0.78 | 26 | empty |
| 3 | 319 | 0.55 | 0.76 | 41 | empty |
| 4 | 163 | 0.47 | 0.76 | 31 | empty |
| 5 | 92 | 0.47 | 0.81 | 19 | empty |
Interfaces
5 interfaces between chains.
- 1–3 · 4259 Ų buried · 65 hydrogen bonds · protein-protein
- 1–2 · 2097 Ų buried · 42 hydrogen bonds · protein-protein
- 2–3 · 1683 Ų buried · 16 hydrogen bonds · protein-protein
- 1–4 · 658 Ų buried · 6 hydrogen bonds · protein-protein
- 3–4 · 373 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 lipid (myristoylation).
Compared structures
- 1QJY · Human rhinovirus 16 coat protein in complex with antiviral compound VP65099 · the same entry in another collection · chain 1 against 1, 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 Q82122
- Elsewhere: RCSB PDB 1QJY · PDBe 1QJY · UniProt Q82122
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