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MolNFT v1 · #185789 · protein

Human connexin 26 dodecamer at 55MM hg PCO2, PH7.4

7QER · Gap junction beta-2 protein: “Human connexin 26 dodecamer at 55MM hg PCO2, PH7.4”. Electron microscopy, 1 ligand (PTY), 20 pockets (best druggability 0.83). MolNFT v1 #185789 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
7QER
Type
protein
Length
2,244 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gap junction beta-2 protein
UniProt
P29033
Ligands
PTY
Pockets
20 · best druggability 0.83

Structure

electron microscopy · 1 distinct chain · 70% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LGap junction beta-2 proteinprotein18770% helix, 5% strandP29033

Ligands and binding sites

  • PTY · Phosphatidylethanolamine · ligand · 12 copies · chains A, F, B, C, D, E, G, L, H, I, J, K
  • LMT · Dodecyl-beta-D-maltoside · additive · 48 copies · chains A, B, C, D, E, F, G, H, I, J, K, L

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17490.830.86107empty
26810.830.8794empty
34740.780.8569empty
44190.770.8662empty
53860.770.8651empty

Interfaces

24 interfaces between chains.

  • D–E · 1515 Ų buried · 21 hydrogen bonds · protein-protein
  • A–F · 1510 Ų buried · 17 hydrogen bonds · protein-protein
  • G–H · 1482 Ų buried · 18 hydrogen bonds · protein-protein
  • G–L · 1480 Ų buried · 18 hydrogen bonds · protein-protein
  • K–L · 1436 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 36 disulfide (disulfide).

Compared structures

  • 7QER · human Connexin 26 dodecamer at 55mm Hg PCO2, pH7.4 · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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