Research workbench
Crystal structure of R. ruber adh-a, mutant Y294F, W295A, F43H, H39Y
Analyse Crystal structure of R. ruber adh-a, mutant Y294F, W295A, F43H, H39Y in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5O8H
- Type
- protein
- Length
- 1,383 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Alcohol dehydrogenase
- UniProt
- A0A1Q8I6M1
- Ligands
- NAD, ZN, K
- Pockets
- 13 · best druggability 0.78
Structure
x-ray diffraction · 2 distinct chains · 28% helix, 25% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Alcohol dehydrogenase | protein | 346 | 28% helix, 25% strand | A0A1Q8I6M1 |
| D | Alcohol dehydrogenase | protein | 345 | 28% helix, 25% strand | A0A1Q8I6M1 |
Ligands and binding sites
- NAD · Nicotinamide-adenine-dinucleotide · ligand · 4 copies · chains A, C, B, D
- ZN · Zinc ion · metal · 8 copies · chains A, B, C, D
- K · Potassium ion · metal · 2 copies · chains A, B, C, D
- GOL · Glycerol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
13 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 701 | 0.78 | 0.83 | 91 | empty |
| 2 | 827 | 0.77 | 0.80 | 76 | NAD |
| 3 | 845 | 0.76 | 0.80 | 76 | ZN, NAD |
| 4 | 800 | 0.76 | 0.80 | 73 | NAD |
| 5 | 752 | 0.75 | 0.80 | 73 | NAD |
Interfaces
6 interfaces between chains.
- B–D · 1504 Ų buried · 21 hydrogen bonds · protein-protein
- A–C · 1465 Ų buried · 18 hydrogen bonds · protein-protein
- A–D · 515 Ų buried · 6 hydrogen bonds · protein-protein
- B–C · 511 Ų buried · 6 hydrogen bonds · protein-protein
- C–D · 442 Ų buried · 3 hydrogen bonds · protein-protein
Compared structures
- 5O8H · Crystal structure of R. ruber ADH-A, mutant Y294F, W295A, F43H, H39Y · 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 A0A1Q8I6M1
- Elsewhere: RCSB PDB 5O8H · PDBe 5O8H · UniProt A0A1Q8I6M1
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