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Cryoem structure of NAV1.7 VSD2 (deactived state) in complex with the gating modifier toxin PROTX2

Analyse Cryoem structure of NAV1.7 VSD2 (deactived state) in complex with the gating… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6N4R
Type
protein
Length
1,942 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NAV1.7 VSD2-navab chimera; BETA/OMEGA-theraphotoxin-TP2A; Fab light chain; Fab heavy chain
UniProt
A8EVM5, Q15858, P83476
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 5 distinct chains · 39% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B, DNAV1.7 VSD2-navab chimeraprotein22574% helix, 0% strandA8EVM5, Q15858
C, ANAV1.7 VSD2-navab chimeraprotein24376% helix, 0% strandA8EVM5, Q15858
E, F, G, HBETA/OMEGA-theraphotoxin-TP2Aprotein300% helix, 33% strandP83476
I, KFab light chainprotein2155% helix, 47% strand—
J, LFab heavy chainprotein2284% helix, 50% strand—

Pockets

20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18720.850.8685empty
27180.730.7971empty
37930.730.7866empty
43770.660.7945empty
52880.630.8033empty

Interfaces

24 interfaces between chains.

  • I–J · 1884 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 1864 Ų buried · 5 hydrogen bonds · protein-protein
  • D–A · 1852 Ų buried · 5 hydrogen bonds · protein-protein
  • K–L · 1842 Ų buried · 10 hydrogen bonds · protein-protein
  • B–A · 1697 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 21 disulfide (disulfide).

Compared structures

  • 6N4R · CryoEM structure of Nav1.7 VSD2 (deactived state) in complex with the gating modifier… · the same entry in another collection · chain A against A, TM-score 1.00

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