Research workbench
SUCCINATE:COENZYME-a transferase (pig heart)
Analyse SUCCINATE:COENZYME-a transferase (pig heart) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1O9L
- Type
- protein
- Length
- 1,782 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Succinyl-COA\:3-ketoacid-coenzyme a transferase
- EC
- 2.8.3.5
- UniProt
- Q29551
- Ligands
- EMC, EMT
- Pockets
- 20 · best druggability 0.84
Structure
x-ray diffraction · 4 distinct chains · 22% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Succinyl-COA\:3-ketoacid-coenzyme a transferase (EC 2.8.3.5) | protein | 468 | 20% helix, 31% strand | Q29551 |
| B | Succinyl-COA\:3-ketoacid-coenzyme a transferase (EC 2.8.3.5) | protein | 425 | 23% helix, 32% strand | Q29551 |
| C | Succinyl-COA\:3-ketoacid-coenzyme a transferase (EC 2.8.3.5) | protein | 425 | 22% helix, 33% strand | Q29551 |
| D | Succinyl-COA\:3-ketoacid-coenzyme a transferase (EC 2.8.3.5) | protein | 464 | 21% helix, 32% strand | Q29551 |
Ligands and binding sites
- EMC · Ethyl mercury ion · ligand · 7 copies · chains A, B, C, D
- EMT · 2-(ethylmercuri-thio)-benzoic acid · 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, 12 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 256 | 0.84 | 0.96 | 37 | empty |
| 2 | 247 | 0.84 | 0.96 | 38 | empty |
| 3 | 528 | 0.73 | 0.81 | 67 | empty |
| 4 | 371 | 0.69 | 0.82 | 46 | empty |
| 5 | 271 | 0.67 | 0.83 | 42 | EMT |
Interfaces
4 interfaces between chains.
- A–B · 2458 Ų buried · 46 hydrogen bonds · protein-protein
- C–D · 2450 Ų buried · 42 hydrogen bonds · protein-protein
- A–C · 462 Ų buried · 5 hydrogen bonds · protein-protein
- B–D · 96 Ų buried · 0 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 Q29551
- Elsewhere: RCSB PDB 1O9L · PDBe 1O9L · UniProt Q29551
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