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Crystal structure of the anti-hinge rabbit antibody 2095-2 in complex with ides hinge peptide

Analyse Crystal structure of the anti-hinge rabbit antibody 2095-2 in complex with ides… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4O4Y
Type
protein
Length
441 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2095-2 light chain; 2095-2 heavy chain; Ides hinge peptide
Pockets
5 · best druggability 0.55

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L2095-2 light chainprotein2198% helix, 51% strand—
H2095-2 heavy chainprotein2158% helix, 51% strand—
AIdes hinge peptideprotein70% helix, 0% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · 5 copies · chains L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12420.550.7737empty
23320.530.7450GOL
31050.360.7419GOL
4610.320.7616empty
5580.250.7213empty

Interfaces

3 interfaces between chains.

  • L–H · 1870 Ų buried · 19 hydrogen bonds · protein-protein
  • H–A · 316 Ų buried · 8 hydrogen bonds · protein-protein
  • L–A · 299 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 2 modified (disulfide, cyclization).

Compared structures

  • 4O4Y · Crystal structure of the anti-hinge rabbit antibody 2095-2 in complex with IDES hinge… · the same entry in another collection · chain L against L, TM-score 1.00

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