Research workbench
Human gabaa receptor ALPHA1-BETA2-GAMMA2 subtype in complex with GABA plus propofol
Analyse Human gabaa receptor ALPHA1-BETA2-GAMMA2 subtype in complex with GABA plus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6X3T
- Type
- protein
- Length
- 2,121 residues
- Chains
- 9
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Gamma-aminobutyric acid receptor subunit beta-2; Gamma-aminobutyric acid receptor subunit…
- UniProt
- P47870, P14867, P18507
- Ligands
- ABU, PFL, NAG, MAN, BMA
- Pockets
- 20 · best druggability 0.84
Structure
electron microscopy · 7 distinct chains · 25% helix, 37% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Gamma-aminobutyric acid receptor subunit beta-2 | protein | 334 | 35% helix, 32% strand | P47870 |
| B, D | Gamma-aminobutyric acid receptor subunit alpha-1 | protein | 338 | 36% helix, 31% strand | P14867 |
| E | Gamma-aminobutyric acid type a receptor subunit gamma-2 | protein | 333 | 36% helix, 34% strand | P18507 |
| I | Kappa Fab light chain | protein | 105 | 3% helix, 45% strand | — |
| J | IGG2B Fab heavy chain | protein | 116 | 3% helix, 52% strand | — |
| L | Kappa Fab light chain | protein | 106 | 0% helix, 45% strand | — |
| K | IGG2B Fab heavy chain | protein | 117 | 3% helix, 51% strand | — |
Ligands and binding sites
- ABU · Gamma-amino-butanoic acid · ligand · 2 copies · chains A, B, C, D
- PFL · 2,6-bis(1-methylethyl)phenol · ligand · 2 copies · chains A, B, C, D
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 12 copies · chains A, B, C, D, E
- MAN · alpha-D-mannopyranose · sugar · 7 copies · chains E, D
- BMA · beta-D-mannopyranose · sugar · 4 copies · chains E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 982 | 0.84 | 0.85 | 93 | PFL |
| 2 | 788 | 0.73 | 0.78 | 77 | empty |
| 3 | 700 | 0.71 | 0.78 | 58 | empty |
| 4 | 623 | 0.70 | 0.78 | 52 | empty |
| 5 | 577 | 0.68 | 0.78 | 59 | empty |
Interfaces
11 interfaces between chains.
- C–D · 2773 Ų buried · 16 hydrogen bonds · protein-protein
- B–C · 2675 Ų buried · 24 hydrogen bonds · protein-protein
- A–B · 2665 Ų buried · 16 hydrogen bonds · protein-protein
- A–E · 2662 Ų buried · 21 hydrogen bonds · protein-protein
- D–E · 2481 Ų buried · 18 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 9 disulfide, 7 glycan (disulfide, N-glycosylation).
Compared structures
- 6X3T · Human GABAA receptor alpha1-beta2-gamma2 subtype in complex with GABA plus propofol · the same entry in another collection · chain K against K, TM-score 1.00
- P47870 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit beta-2… · a predicted model of the same protein · chain A against A, TM-score 0.99
- P18507 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit gamma-2… · a predicted model of the same protein · chain E against A, TM-score 0.98
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 P47870
- Every structure of UniProt P14867
- Every structure of UniProt P18507
- Elsewhere: RCSB PDB 6X3T · PDBe 6X3T · UniProt P47870 · UniProt P14867 · UniProt P18507
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