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Structural snapshots of intermediates in the gating of a K+ channel

Analyse Structural snapshots of intermediates in the gating of a K+ channel in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7M2I
Type
protein
Length
526 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Monoclonal antibody (IgG) against kcsa, Fab heavy chain; Monoclonal antibody (IgG)…
UniProt
P0A334
Ligands
F09, 1EM, K
Pockets
5 · best druggability 0.68

Structure

x-ray diffraction · 3 distinct chains · 16% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMonoclonal antibody (IgG) against kcsa, Fab heavy chainprotein2193% helix, 50% strand—
BMonoclonal antibody (IgG) against kcsa, Fab light chainprotein2116% helix, 51% strand—
CPH-gated potassium channel kcsaprotein9670% helix, 0% strandP0A334

Ligands and binding sites

  • F09 · Nonan-1-ol · ligand · chains A, C
  • 1EM · (1S)-2-hydroxy-1-[(nonanoyloxy)methyl]ethyl myristate · ligand · chains C
  • K · Potassium ion · metal · 6 copies · chains C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17660.680.7559empty
2680.530.8718empty
3580.520.8714empty
41840.490.7628empty
5760.370.7718empty

Interfaces

3 interfaces between chains.

  • A–B · 1838 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 467 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 438 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 7M2I · Structural Snapshots of Intermediates in the Gating of a K+ Channel · the same entry in another collection · chain A against A, TM-score 1.00

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