Research workbench
Oxa-48 in complex with compound 21B
Analyse Oxa-48 in complex with compound 21B in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5QAQ
- Type
- protein
- Length
- 968 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Beta-lactamase
- EC
- 3.5.2.6
- UniProt
- Q6XEC0
- Ligands
- S1C, CL
- Pockets
- 9 · best druggability 0.73
Structure
x-ray diffraction · 1 distinct chain · 40% helix, 20% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Beta-lactamase (EC 3.5.2.6) | protein | 242 | 40% helix, 20% strand | Q6XEC0 |
Ligands and binding sites
- S1C · 3-(4-acetamidophenyl)benzoic acid · ligand · 3 copies · chains B, C, D
- CL · Chloride ion · ion · 2 copies · chains A, B
- EDO · 1,2-ethanediol · additive · 4 copies · chains A, B, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 572 | 0.73 | 0.81 | 71 | EDO |
| 2 | 473 | 0.71 | 0.81 | 57 | empty |
| 3 | 280 | 0.65 | 0.81 | 39 | empty |
| 4 | 172 | 0.48 | 0.77 | 30 | empty |
| 5 | 53 | 0.43 | 0.83 | 14 | empty |
Interfaces
4 interfaces between chains.
- A–B · 434 Ų buried · 3 hydrogen bonds · protein-protein
- B–C · 341 Ų buried · 6 hydrogen bonds · protein-protein
- C–D · 286 Ų buried · 3 hydrogen bonds · protein-protein
- A–C · 265 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 modified (carboxylation).
Compared structures
- 5QAQ · OXA-48 IN COMPLEX WITH COMPOUND 21b · 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 Q6XEC0
- Elsewhere: RCSB PDB 5QAQ · PDBe 5QAQ · UniProt Q6XEC0
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