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X-ray structure of amyloid beta PEPTIDE:ANTIBODY (ABETA1-7:10D5) complex

Analyse X-ray structure of amyloid beta PEPTIDE:ANTIBODY (ABETA1-7:10D5) complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3IFO
Type
protein
Length
880 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
10D5 Fab antibody heavy chain; 10D5 Fab antibody light chain; Amyloid beta A4 protein
UniProt
P05067
Pockets
9 · best druggability 0.82

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H, A10D5 Fab antibody heavy chainprotein2167% helix, 50% strand—
L, B10D5 Fab antibody light chainprotein2186% helix, 51% strand—
P, QAmyloid beta A4 proteinprotein60% helix, 17% strandP05067

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110370.820.84113empty
21860.480.7636empty
31760.460.7521empty
41270.450.7728empty
5680.410.8016empty

Interfaces

10 interfaces between chains.

  • A–B · 1839 Ų buried · 19 hydrogen bonds · protein-protein
  • H–L · 1833 Ų buried · 15 hydrogen bonds · protein-protein
  • L–B · 518 Ų buried · 4 hydrogen bonds · protein-protein
  • A–Q · 385 Ų buried · 11 hydrogen bonds · protein-protein
  • H–P · 358 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 3IFO · X-ray structure of amyloid beta peptide:antibody (Abeta1-7:10D5) complex · the same entry in another collection · chain Q against Q, TM-score 1.00
  • P05067 · AlphaFold monomer V2.0 prediction for amyloid-beta precursor protein (P05067) · a predicted model of the same protein · chain P against A, TM-score 0.66

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