Research workbench
Impa metallopeptidase from pseudomonas aeruginosa
Analyse Impa metallopeptidase from pseudomonas aeruginosa in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5KDW
- Type
- protein
- Length
- 1,766 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Metallopeptidase
- UniProt
- Q9I5W4
- Ligands
- ZN, PO4
- Pockets
- 17 · best druggability 0.65
Structure
x-ray diffraction · 1 distinct chain · 40% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Metallopeptidase | protein | 883 | 40% helix, 15% strand | Q9I5W4 |
Ligands and binding sites
- ZN · Zinc ion · metal · 2 copies · chains A, B
- PO4 · Phosphate ion · ion · 7 copies · chains A, B
- EDO · 1,2-ethanediol · additive · 42 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
17 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 465 | 0.65 | 0.77 | 61 | EDO |
| 2 | 365 | 0.63 | 0.79 | 38 | empty |
| 3 | 282 | 0.58 | 0.78 | 37 | EDO |
| 4 | 182 | 0.55 | 0.80 | 27 | empty |
| 5 | 175 | 0.54 | 0.80 | 25 | empty |
Interfaces
1 interface between chains.
- A–B · 1029 Ų buried · 16 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide (disulfide).
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 Q9I5W4
- Elsewhere: RCSB PDB 5KDW · PDBe 5KDW · UniProt Q9I5W4
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