Research workbench
Complex of H275Y mutant variant of neuraminidase from H1N1 influenza virus with oseltamivir
Analyse Complex of H275Y mutant variant of neuraminidase from H1N1 influenza virus with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5NWE
- Type
- protein
- Length
- 1,552 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Neuraminidase
- EC
- 3.2.1.18
- UniProt
- C9EKP8
- Ligands
- G39, NAG, BMA, MAN, FUC, CA
- Pockets
- 17 · best druggability 0.62
Structure
x-ray diffraction · 1 distinct chain · 4% helix, 44% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Neuraminidase (EC 3.2.1.18) | protein | 388 | 4% helix, 44% strand | C9EKP8 |
Ligands and binding sites
- G39 · (3R,4R,5S)-4-(acetylamino)-5-amino-3-(pentan-3-yloxy) cyclohex-1-ene-1-carboxylic acid · ligand · 4 copies · chains A, B, C, D
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 14 copies · chains A, C, B, D
- BMA · beta-D-mannopyranose · sugar
- MAN · alpha-D-mannopyranose · sugar
- FUC · alpha-L-fucopyranose · sugar · chains A, B
- CA · Calcium ion · metal · 8 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
17 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 272 | 0.62 | 0.80 | 43 | G39 |
| 2 | 270 | 0.62 | 0.80 | 43 | G39 |
| 3 | 270 | 0.61 | 0.80 | 44 | G39 |
| 4 | 264 | 0.60 | 0.79 | 44 | G39 |
| 5 | 169 | 0.57 | 0.81 | 23 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1604 Ų buried · 23 hydrogen bonds · protein-protein
- B–C · 1595 Ų buried · 24 hydrogen bonds · protein-protein
- C–D · 1593 Ų buried · 22 hydrogen bonds · protein-protein
- A–D · 1571 Ų buried · 23 hydrogen bonds · protein-protein
- B–D · 17 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 32 disulfide, 12 glycan (disulfide, N-glycosylation).
Compared structures
- 5NWE · Complex of H275Y mutant variant of neuraminidase from H1N1 influenza virus with… · 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 C9EKP8
- Elsewhere: RCSB PDB 5NWE · PDBe 5NWE · UniProt C9EKP8
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