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Aplysia SLO1 with barium

Analyse Aplysia SLO1 with barium in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7RK6
Type
protein
Length
3,564 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bk channel
UniProt
Q5QJC5
Ligands
PGW, BA, K
Pockets
20 · best druggability 0.76

Structure

electron microscopy · 1 distinct chain · 47% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DBk channelprotein89147% helix, 13% strandQ5QJC5

Ligands and binding sites

  • PGW · (1R)-2-{[(S)-{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy) phosphoryl]oxy}-1-[(hexadecanoyloxy)methyl]ethyl (9Z)-octadec-9-enoate · ligand · 16 copies · chains A, B, C, D
  • BA · Barium ion · metal · 8 copies · chains A, B, C, D
  • K · Potassium ion · metal · 3 copies · chains A, B, C, D

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
16820.760.8168empty
2780.740.9821empty
3760.740.9821empty
4730.740.9820empty
5780.730.9722empty

Interfaces

6 interfaces between chains.

  • C–D · 1738 Ų buried · 10 hydrogen bonds · protein-protein
  • A–D · 1732 Ų buried · 10 hydrogen bonds · protein-protein
  • B–C · 1732 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 1729 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 43 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 7RK6 · Aplysia Slo1 with Barium · the same entry in another collection · chain A against A, TM-score 1.00

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