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MolNFT v1 · #16845 · protein

Antibody multispecificity mediated by conformational diversity

1OAY · Immunoglobulin E: “Antibody multispecificity mediated by conformational diversity”. X-ray diffraction, 1 ligand (FUR), 7 pockets (best druggability 0.64). MolNFT v1 #16845 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
1OAY
Type
protein
Length
634 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Immunoglobulin E
Ligands
FUR
Pockets
7 · best druggability 0.64

Structure

x-ray diffraction · 5 distinct chains · 1% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H, JImmunoglobulin Eprotein1215% helix, 49% strand—
LImmunoglobulin Eprotein1080% helix, 44% strand—
MImmunoglobulin Eprotein850% helix, 33% strand—
NImmunoglobulin Eprotein1070% helix, 50% strand—
OImmunoglobulin Eprotein920% helix, 33% strand—

Ligands and binding sites

  • FUR · Furazolidone · ligand · 2 copies · chains H, L, O, J, M, N

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

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1770.640.9123empty
21970.570.8032FUR
32420.570.7824empty
41540.530.7929FUR
51540.430.7526empty

Interfaces

6 interfaces between chains.

  • J–N · 934 Ų buried · 10 hydrogen bonds · protein-protein
  • H–L · 931 Ų buried · 9 hydrogen bonds · protein-protein
  • H–O · 235 Ų buried · 2 hydrogen bonds · protein-protein
  • J–M · 202 Ų buried · 2 hydrogen bonds · protein-protein
  • M–N · 41 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 1OAY · Antibody multispecificity mediated by conformational diversity · the same entry in another collection · chain H against H, TM-score 1.00

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