Research workbench
Activated turkey BETA1 adrenoceptor with bound partial agonist dobutamine and nanobody NB6B9
Analyse Activated turkey BETA1 adrenoceptor with bound partial agonist dobutamine and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6H7L
- Type
- protein
- Length
- 1,030 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Thioredoxin 1; Beta-1 adrenergic receptor; Camelid antibody fragment NB6B9
- UniProt
- P0AA25, P07700
- Ligands
- 2CV, Y00, NA
- Pockets
- 13 · best druggability 0.77
Structure
x-ray diffraction · 5 distinct chains · 61% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| E | Thioredoxin 1 | protein | 107 | 36% helix, 27% strand | P0AA25 |
| A | Beta-1 adrenergic receptor | protein | 291 | 82% helix, 0% strand | P07700 |
| C, D | Camelid antibody fragment NB6B9 | protein | 120 | 3% helix, 54% strand | — |
| F | Thioredoxin 1 | protein | 107 | 35% helix, 28% strand | P0AA25 |
| B | Beta-1 adrenergic receptor | protein | 285 | 84% helix, 0% strand | P07700 |
Ligands and binding sites
- 2CV · Hega-10 · ligand · 9 copies · chains E, A, B
- Y00 · Dobutamine · ligand · 2 copies · chains A, B
- NA · Sodium ion · metal · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1126 | 0.77 | 0.79 | 92 | 2CV |
| 2 | 450 | 0.73 | 0.82 | 53 | Y00 |
| 3 | 390 | 0.73 | 0.83 | 51 | Y00 |
| 4 | 336 | 0.59 | 0.77 | 38 | empty |
| 5 | 289 | 0.58 | 0.77 | 33 | empty |
Interfaces
7 interfaces between chains.
- A–C · 1216 Ų buried · 13 hydrogen bonds · protein-protein
- B–D · 1197 Ų buried · 13 hydrogen bonds · protein-protein
- A–B · 573 Ų buried · 2 hydrogen bonds · protein-protein
- F–B · 205 Ų buried · 2 hydrogen bonds · protein-protein
- A–F · 158 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide (disulfide).
Compared structures
- 6H7L · ACTIVATED TURKEY BETA1 ADRENOCEPTOR WITH BOUND PARTIAL AGONIST DOBUTAMINE AND NANOBODY… · the same entry in another collection · chain D against D, TM-score 1.00
- P0AA25 · AlphaFold monomer V2.0 prediction for thioredoxin 1 (P0AA25) · a predicted model of the same protein · chain F against A, TM-score 0.97
- P07700 · AlphaFold monomer V2.0 prediction for beta-1 adrenergic receptor (P07700) · a predicted model of the same protein · chain B against A, TM-score 0.90
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 P0AA25
- Every structure of UniProt P07700
- Elsewhere: RCSB PDB 6H7L · PDBe 6H7L · UniProt P0AA25 · UniProt P07700
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.