Research workbench
E. COLI 2-oxoglutarate dehydrogenase (E1o)
Analyse E. COLI 2-oxoglutarate dehydrogenase (E1o) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2JGD
- Type
- protein
- Length
- 1,619 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.6
- Source
- ESCHERICHIA COLI
- Molecule
- 2-oxoglutarate dehydrogenase E1 component
- EC
- 1.2.4.2
- UniProt
- P0AFG3
- Ligands
- AMP
- Pockets
- 20 · best druggability 0.82
Structure
x-ray diffraction · resolution 2.6 · 2 distinct chains · 44% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 2-oxoglutarate dehydrogenase E1 component (EC 1.2.4.2) | protein | 812 | 43% helix, 15% strand | P0AFG3 |
| B | 2-oxoglutarate dehydrogenase E1 component (EC 1.2.4.2) | protein | 807 | 45% helix, 15% strand | P0AFG3 |
Ligands and binding sites
- AMP · Adenosine monophosphate · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 953 | 0.82 | 0.84 | 132 | empty |
| 2 | 927 | 0.74 | 0.78 | 84 | empty |
| 3 | 50 | 0.70 | 0.98 | 26 | empty |
| 4 | 50 | 0.69 | 0.98 | 17 | empty |
| 5 | 472 | 0.63 | 0.76 | 55 | AMP |
Interfaces
1 interface between chains.
- A–B · 2907 Ų buried · 44 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 P0AFG3
- Elsewhere: RCSB PDB 2JGD · PDBe 2JGD · UniProt P0AFG3
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