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MolNFT v2 · #218953 · protein

CryoEM structure of human rho1 GABAA receptor in complex with pregnenolone sulfate

8RH9 · Gamma-aminobutyric acid receptor subunit rho-1: “CryoEM structure of human rho1 GABAA receptor in complex with pregnenolone sulfate”. Electron microscopy at 3.21, 5 ligands (D10, D12, A8W), 20 pockets (best druggability 0.86).…

PDB
8RH9
Type
protein
Length
1,665 residues
Chains
5
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.21
Source
Homo sapiens
Molecule
Gamma-aminobutyric acid receptor subunit rho-1
UniProt
P24046
Ligands
D10, D12, A8W, NAG, CL
Pockets
20 · best druggability 0.86

Structure

electron microscopy · resolution 3.21 · 1 distinct chain · 37% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, EGamma-aminobutyric acid receptor subunit rho-1protein33337% helix, 31% strandP24046

Ligands and binding sites

  • D10 · Decane · ligand · 7 copies · chains A, E, C, D
  • D12 · Dodecane · ligand · 3 copies · chains A, D
  • A8W · Pregnenolone sulfate · ligand · chains A, B, C, D, E
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 10 copies · chains A, B, C, D, E
  • CL · Chloride ion · ion · chains B, C
  • OCT · N-octane · additive · 16 copies · chains A, B, C, D, E
  • HEX · Hexane · additive · 13 copies · chains A, B, C, D, 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, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110430.860.8796A8W
22860.780.8937empty
36540.780.8392empty
42810.770.8936empty
52740.760.8838empty

Interfaces

5 interfaces between chains.

  • C–D · 2730 Ų buried · 20 hydrogen bonds · protein-protein
  • D–E · 2711 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 2702 Ų buried · 18 hydrogen bonds · protein-protein
  • A–E · 2701 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 2651 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • P24046 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit rho-1… · a predicted model of the same protein · chain D against A, TM-score 0.88

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