MolNFT v1 · #9597 · protein
Neurolysin (endopeptidase 24.16) crystal structure
1I1I: “Neurolysin (endopeptidase 24.16) crystal structure”. X-ray diffraction, 1 ligand (ZN), 3 pockets (best druggability 0.75). MolNFT v1 #9597 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1I1I
- Type
- protein
- Length
- 665 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Neurolysin
- EC
- 3.4.24.16
- UniProt
- P42676
- Ligands
- ZN
- Pockets
- 3 · best druggability 0.75
Structure
x-ray diffraction · 1 distinct chain · 59% helix, 7% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| P | Neurolysin (EC 3.4.24.16) | protein | 665 | 59% helix, 7% strand | P42676 |
Ligands and binding sites
- ZN · Zinc ion · metal · 2 copies · chains P
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1032 | 0.75 | 0.77 | 88 | empty |
| 2 | 835 | 0.74 | 0.79 | 83 | empty |
| 3 | 69 | 0.42 | 0.81 | 18 | empty |
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 P42676
- Elsewhere: RCSB PDB 1I1I · PDBe 1I1I · UniProt P42676
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