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Crystal structure of the complex between CNTO607 Fab and il-13

Analyse Crystal structure of the complex between CNTO607 Fab and il-13 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3G6D
Type
protein
Length
539 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CNTO607 Fab light chain; CNTO607 Fab heavy chain; Interleukin-13
UniProt
P35225
Ligands
SO4
Pockets
7 · best druggability 0.55

Structure

x-ray diffraction · 3 distinct chains · 15% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LCNTO607 Fab light chainprotein2108% helix, 49% strand—
HCNTO607 Fab heavy chainprotein2237% helix, 48% strand—
AInterleukin-13protein10647% helix, 6% strandP35225

Ligands and binding sites

  • SO4 · Sulfate ion · ion · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14200.550.7355empty
21490.460.7726empty
3970.380.7619empty
41070.370.7421empty
5810.320.7424empty

Interfaces

3 interfaces between chains.

  • L–H · 1741 Ų buried · 15 hydrogen bonds · protein-protein
  • L–A · 540 Ų buried · 11 hydrogen bonds · protein-protein
  • H–A · 476 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 3G6D · Crystal structure of the complex between CNTO607 Fab and IL-13 · the same entry in another collection · chain L against L, TM-score 1.00
  • P35225 · AlphaFold monomer V2.0 prediction for interleukin-13 (P35225) · a predicted model of the same protein · chain A against A, TM-score 0.87

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