Research workbench
Crystal structure of yeast COQ5 in the apo form
Analyse Crystal structure of yeast COQ5 in the apo form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4OBX
- Type
- protein
- Length
- 940 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
- EC
- 2.1.1.201
- UniProt
- P49017
- Ligands
- TAM
- Pockets
- 10 · best druggability 0.74
Structure
x-ray diffraction · 1 distinct chain · 49% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D, C, B | 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial (EC 2.1.1.201) | protein | 235 | 49% helix, 22% strand | P49017 |
Ligands and binding sites
- TAM · Tris(hydroxyethyl)aminomethane · ligand · 2 copies · chains A, D, C, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1111 | 0.74 | 0.77 | 89 | empty |
| 2 | 629 | 0.69 | 0.77 | 75 | empty |
| 3 | 255 | 0.66 | 0.83 | 39 | empty |
| 4 | 239 | 0.66 | 0.83 | 36 | empty |
| 5 | 68 | 0.48 | 0.83 | 20 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1057 Ų buried · 0 hydrogen bonds · protein-protein
- D–C · 1051 Ų buried · 0 hydrogen bonds · protein-protein
- A–D · 261 Ų buried · 3 hydrogen bonds · protein-protein
- C–B · 258 Ų buried · 4 hydrogen bonds · protein-protein
- A–C · 41 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 P49017
- Elsewhere: RCSB PDB 4OBX · PDBe 4OBX · UniProt P49017
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