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MolNFT v1 · #151661 · protein

Cryoem structure of human full-length ALPHA1BETA3GAMMA2L GABA(A)R in complex with picrotoxin and megabody MB38.

6HUG · Gamma-aminobutyric acid receptor subunit alpha-1: “Cryoem structure of human full-length ALPHA1BETA3GAMMA2L GABA(A)R in complex with picrotoxin and megabody…”. Electron microscopy, 5 ligands (PIO, RI5, NAG), 20 pockets (best…

PDB
6HUG
Type
protein
Length
1,815 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gamma-aminobutyric acid receptor subunit alpha-1; Gamma-aminobutyric acid receptor…
UniProt
P08219, P28472, P18507
Ligands
PIO, RI5, NAG, MAN, BMA
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 6 distinct chains · 32% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGamma-aminobutyric acid receptor subunit alpha-1protein34733% helix, 29% strandP08219
BGamma-aminobutyric acid receptor subunit beta-3protein33636% helix, 30% strandP28472
CGamma-aminobutyric acid receptor subunit gamma-2protein33032% helix, 32% strandP18507
DGamma-aminobutyric acid receptor subunit alpha-1protein34734% helix, 28% strandP08219
EGamma-aminobutyric acid receptor subunit beta-3protein33437% helix, 31% strandP28472
GMegabody MB38protein1215% helix, 46% strand—

Ligands and binding sites

  • PIO · [(2R)-2-octanoyloxy-3-[oxidanyl-[(1R,2R,3S,4R,5R,6S)-2, 3,6-tris(oxidanyl)-4,5-diphosphonooxy-cyclohexyl]oxy-phosphoryl]oxy-propyl] octanoate · ligand · 2 copies · chains A, D
  • RI5 · (1aR,2aR,3S,6R,6aS,8aS,8bR,9R)-2a-hydroxy-8b-methyl-9-(prop-1-en-2-yl)hexahydro-3,6-methano-1,5,7-trioxacyclopenta[ij]c yclopropa[a]azulene-4,8(3H)-dione · ligand · chains A, B, C, D, E
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 14 copies · chains A, B, C, D, E
  • MAN · alpha-D-mannopyranose · sugar · 14 copies · chains C, D, B, A, E
  • BMA · beta-D-mannopyranose · sugar · 4 copies · chains C, B, 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.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19420.840.85104RI5
29950.820.83114empty
37670.740.7980empty
45030.740.8267empty
54740.710.8158empty

Interfaces

8 interfaces between chains.

  • A–B · 3059 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 3018 Ų buried · 19 hydrogen bonds · protein-protein
  • D–E · 2981 Ų buried · 17 hydrogen bonds · protein-protein
  • A–E · 2908 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 2887 Ų buried · 30 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 glycan, 6 disulfide (N-glycosylation, disulfide).

Compared structures

  • 6HUG · CryoEM structure of human full-length alpha1beta3gamma2L GABA(A)R in complex with… · the same entry in another collection · chain G against G, TM-score 1.00
  • P18507 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit gamma-2… · a predicted model of the same protein · chain C against A, TM-score 0.99
  • P08219 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit alpha-1… · a predicted model of the same protein · chain A against A, TM-score 0.99
  • P28472 · AlphaFold monomer V2.0 prediction for gamma-aminobutyric acid receptor subunit beta-3… · a predicted model of the same protein · chain E against A, TM-score 0.98

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