Research workbench
Neprilysin complexed with LBQ657
Analyse Neprilysin complexed with LBQ657 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5JMY
- Type
- protein
- Length
- 1,392 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Neprilysin
- EC
- 3.4.24.11
- UniProt
- P08473
- Ligands
- 6LD, NAG, ZN
- Pockets
- 20 · best druggability 0.83
Structure
x-ray diffraction · 1 distinct chain · 59% helix, 8% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Neprilysin (EC 3.4.24.11) | protein | 696 | 59% helix, 8% strand | P08473 |
Ligands and binding sites
- 6LD · Sacubitrilat · ligand · 2 copies · chains A, B
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 10 copies · chains A, B
- ZN · Zinc ion · metal · 2 copies · chains A, 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, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1143 | 0.83 | 0.84 | 98 | empty |
| 2 | 171 | 0.68 | 0.87 | 31 | ZN, 6LD |
| 3 | 148 | 0.67 | 0.88 | 29 | 6LD |
| 4 | 364 | 0.65 | 0.80 | 53 | empty |
| 5 | 156 | 0.56 | 0.81 | 25 | empty |
Interfaces
1 interface between chains.
- A–B · 1004 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 12 disulfide, 8 glycan (disulfide, N-glycosylation).
Compared structures
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 P08473
- Elsewhere: RCSB PDB 5JMY · PDBe 5JMY · UniProt P08473
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