Research workbench
Human rhinovirus 16 coat protein in complex with antiviral compound WIN68934
Analyse Human rhinovirus 16 coat protein in complex with antiviral compound WIN68934 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1QJX
- 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
- W02, MYR, ZN
- Pockets
- 13 · best druggability 0.76
Structure
x-ray diffraction · 4 distinct chains · 13% 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 | 13% 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
- W02 · 2,6-dimethyl-1-(3-[3-methyl-5-isoxazolyl]-propanyl)-4-[4-methyl-2H-tetrazol-2-yl]-phenol · ligand · chains 1
- 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
13 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 425 | 0.76 | 0.85 | 64 | W02 |
| 2 | 233 | 0.55 | 0.78 | 26 | empty |
| 3 | 288 | 0.55 | 0.76 | 36 | empty |
| 4 | 93 | 0.47 | 0.81 | 17 | empty |
| 5 | 148 | 0.45 | 0.76 | 30 | empty |
Interfaces
5 interfaces between chains.
- 1–3 · 4232 Ų buried · 65 hydrogen bonds · protein-protein
- 1–2 · 2093 Ų buried · 45 hydrogen bonds · protein-protein
- 2–3 · 1686 Ų buried · 17 hydrogen bonds · protein-protein
- 1–4 · 664 Ų buried · 8 hydrogen bonds · protein-protein
- 3–4 · 370 Ų buried · 6 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 lipid (myristoylation).
Compared structures
- 1QJX · Human rhinovirus 16 coat protein in complex with antiviral compound WIN68934 · 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 1QJX · PDBe 1QJX · UniProt Q82122
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