Research workbench
Low resolution crystal structure of the bacterial multidrug efflux transporter acrb in the presence of cadmium
Analyse Low resolution crystal structure of the bacterial multidrug efflux transporter… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6NZI
- Type
- protein
- Length
- 1,011 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Efflux pump membrane transporter
- UniProt
- E2QH56
- Ligands
- CD
- Pockets
- 12 · best druggability 0.85
Structure
x-ray diffraction · 1 distinct chain · 50% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Efflux pump membrane transporter | protein | 1011 | 50% helix, 15% strand | E2QH56 |
Ligands and binding sites
- CD · Cadmium ion · metal · 2 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 628 | 0.85 | 0.89 | 86 | empty |
| 2 | 253 | 0.69 | 0.85 | 46 | empty |
| 3 | 481 | 0.69 | 0.79 | 60 | empty |
| 4 | 51 | 0.65 | 0.95 | 19 | empty |
| 5 | 201 | 0.62 | 0.82 | 29 | CD |
Compared structures
- 6NZI · Low resolution crystal structure of the bacterial multidrug efflux transporter AcrB in… · 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 E2QH56
- Elsewhere: RCSB PDB 6NZI · PDBe 6NZI · UniProt E2QH56
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