Research workbench
Structure of apo form of Vibrio cholerae CqsA
Analyse Structure of apo form of Vibrio cholerae CqsA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2WK7
- Type
- protein
- Length
- 766 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.5
- Source
- VIBRIO CHOLERAE O1 BIOVAR EL TOR
- Molecule
- Cai-1 autoinducer synthase
- EC
- 2.3.-.-
- UniProt
- Q9KM65
- Ligands
- SO4
- Pockets
- 10 · best druggability 0.78
Structure
x-ray diffraction · resolution 2.5 · 2 distinct chains · 44% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cai-1 autoinducer synthase (EC 2.3.-.-) | protein | 386 | 43% helix, 14% strand | Q9KM65 |
| B | Cai-1 autoinducer synthase (EC 2.3.-.-) | protein | 380 | 44% helix, 15% strand | Q9KM65 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 324 | 0.78 | 0.89 | 58 | SO4 |
| 2 | 313 | 0.78 | 0.89 | 57 | SO4 |
| 3 | 550 | 0.71 | 0.80 | 69 | empty |
| 4 | 121 | 0.70 | 0.91 | 25 | empty |
| 5 | 133 | 0.69 | 0.90 | 35 | empty |
Interfaces
1 interface between chains.
- A–B · 3898 Ų buried · 33 hydrogen bonds · protein-protein
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 Q9KM65
- Elsewhere: RCSB PDB 2WK7 · PDBe 2WK7 · UniProt Q9KM65
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