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Structure antibody F9 in complex with methylated peptide

Analyse Structure antibody F9 in complex with methylated peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6LDV
Type
protein
Length
424 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Oryctolagus cuniculus; SYNTHETIC CONSTRUCT
Molecule
Fab heavy chain; Fab light chain; Gly-M3L-gly-gly-thr-tyr-pro
Ligands
IOD
Pockets
3 · best druggability 0.62

Structure

x-ray diffraction · resolution 1.9 · 3 distinct chains · 7% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HFab heavy chainprotein2036% helix, 53% strand—
LFab light chainprotein2147% helix, 53% strand—
PGly-M3L-gly-gly-thr-tyr-proprotein70% helix, 0% strand—

Ligands and binding sites

  • IOD · Iodide ion · ion · 8 copies · chains H, L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15750.620.7457empty
2610.460.8422IOD
3540.270.7415empty

Interfaces

3 interfaces between chains.

  • H–L · 1766 Ų buried · 14 hydrogen bonds · protein-protein
  • H–P · 535 Ų buried · 11 hydrogen bonds · protein-protein
  • L–P · 211 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 1 modified (disulfide, methylation).

Compared structures

  • 6LDV · Structure antibody F9 in complex with methylated peptide · the same entry in another collection · chain H against H, TM-score 1.00

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