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Structure of pyroglutamate-abeta-specific Fab C#17 in complex with human abeta-PE3-12PEGB

Analyse Structure of pyroglutamate-abeta-specific Fab C#17 in complex with human… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5MY4
Type
protein
Length
441 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab C#17 light chain; Fab C#17 heavy chain; Pyroglutamate-abeta PE3-12-pegb
Pockets
4 · best druggability 0.51

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab C#17 light chainprotein2186% helix, 51% strand—
BFab C#17 heavy chainprotein2177% helix, 56% strand—
CPyroglutamate-abeta PE3-12-pegbprotein60% helix, 33% strand—

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12930.510.7442empty
2580.500.8619empty
31200.410.7624empty
4630.300.7418empty

Interfaces

3 interfaces between chains.

  • A–B · 1793 Ų buried · 13 hydrogen bonds · protein-protein
  • B–C · 511 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 150 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 modified (disulfide, cyclization).

Compared structures

  • 5MY4 · Structure of Pyroglutamate-Abeta-specific Fab c#17 in complex with human Abeta-pE3-12PEGb · the same entry in another collection · chain A against A, TM-score 1.00

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