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Fab fragment. abvance: increasing our knowledge of antibody structural space to enable faster and better decision making in antibody drug discovery

Analyse Fab fragment. abvance: increasing our knowledge of antibody structural space to… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6EMJ
Type
protein
Length
854 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab heavy chain; Fab light chain
Ligands
NA
Pockets
13 · best druggability 0.70

Structure

x-ray diffraction · 4 distinct chains · 7% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab heavy chainprotein2128% helix, 54% strand—
BFab light chainprotein2135% helix, 51% strand—
HFab heavy chainprotein2188% helix, 53% strand—
LFab light chainprotein2116% helix, 52% strand—

Ligands and binding sites

  • NA · Sodium ion · metal · chains A

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

Pockets

13 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15410.700.8075empty
23970.630.7836empty
31450.540.8125empty
41510.510.8042empty
51300.510.8023empty

Interfaces

5 interfaces between chains.

  • H–L · 1922 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1807 Ų buried · 17 hydrogen bonds · protein-protein
  • B–L · 719 Ų buried · 13 hydrogen bonds · protein-protein
  • A–L · 57 Ų buried · 1 hydrogen bond · protein-protein
  • B–H · 22 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6EMJ · FAB Fragment. AbVance: Increasing our knowledge of antibody structural space to enable… · the same entry in another collection · chain A against A, TM-score 1.00

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