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Structure of homomeric LRRC8A volume-regulated anion channel in complex with synthetic nanobody SB4 at 1:0.5 ratio

Analyse Structure of homomeric LRRC8A volume-regulated anion channel in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7P60
Type
protein
Length
4,680 residues
Chains
9
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Volume-regulated anion channel subunit LRRC8A; Synthetic nanobody SB4
UniProt
Q80WG5
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 2 distinct chains · 37% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FVolume-regulated anion channel subunit LRRC8Aprotein71843% helix, 12% strandQ80WG5
G, I, HSynthetic nanobody SB4protein1242% helix, 52% strand—

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111990.850.86125empty
2960.770.9724empty
3920.770.9721empty
4880.750.9623empty
5650.750.9818empty

Interfaces

12 interfaces between chains.

  • C–D · 2840 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 2820 Ų buried · 24 hydrogen bonds · protein-protein
  • E–F · 2709 Ų buried · 23 hydrogen bonds · protein-protein
  • B–C · 1261 Ų buried · 11 hydrogen bonds · protein-protein
  • A–F · 1246 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 21 disulfide (disulfide).

Compared structures

  • 7P60 · Structure of homomeric LRRC8A Volume-Regulated Anion Channel in complex with synthetic… · the same entry in another collection · chain I against I, TM-score 1.00
  • Q80WG5 · AlphaFold monomer V2.0 prediction for volume-regulated anion channel subunit LRRC8A… · a predicted model of the same protein · chain A against A, TM-score 0.90

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