Research workbench
E. COLI gyrb ATPase domain in complex with 3,4-dihydroxyacetophenone
Analyse E. COLI gyrb ATPase domain in complex with 3,4-dihydroxyacetophenone in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7DQJ
- Type
- protein
- Length
- 373 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- A0A4S5B230
- Ligands
- HFO, AX7, PO4
Structure
x-ray diffraction · 2 distinct chains.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 185 | — | A0A4S5B230 |
| B | — | protein | 188 | — | A0A4S5B230 |
Ligands and binding sites
- HFO · 1-[3,4-bis(oxidanyl)phenyl]ethanone · ligand · 2 copies · chains A, B
- AX7 · 1H-benzimidazol-2-amine · ligand · chains A, B
- PO4 · Phosphate ion · ion · 3 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7DQJ · E. coli GyrB ATPase domain in complex with 3,4-Dihydroxyacetophe · 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 A0A4S5B230
- Elsewhere: RCSB PDB 7DQJ · PDBe 7DQJ · UniProt A0A4S5B230
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