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Crystal structure of the complex between il-13 and M1295 Fab

Analyse Crystal structure of the complex between il-13 and M1295 Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PS4
Type
protein
Length
513 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
M1295 light chain; M1295 heavy chain; Interleukin-13
UniProt
P35225
Pockets
5 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 13% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LM1295 light chainprotein2136% helix, 51% strand—
HM1295 heavy chainprotein2245% helix, 50% strand—
AInterleukin-13protein7659% helix, 0% strandP35225

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15240.610.7560empty
2540.530.8922empty
32180.500.7538empty
4930.400.7723empty
5860.320.7418empty

Interfaces

3 interfaces between chains.

  • L–H · 1850 Ų buried · 13 hydrogen bonds · protein-protein
  • H–A · 478 Ų buried · 9 hydrogen bonds · protein-protein
  • L–A · 206 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 1 modified (disulfide, cyclization).

Compared structures

  • 4PS4 · Crystal structure of the complex between IL-13 and M1295 FAB · 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 0.94

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