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Crystal structure of the omalizumab Fab Ser81Arg, Gln83Arg and Leu158Pro light chain mutant

Analyse Crystal structure of the omalizumab Fab Ser81Arg, Gln83Arg and Leu158Pro light… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6TCR
Type
protein
Length
428 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.45
Source
Homo sapiens
Molecule
Omalizumab Fab Ser81Arg, Gln83Arg and Leu158Pro light chain mutant
Pockets
3 · best druggability 0.61

Structure

x-ray diffraction · resolution 1.45 · 2 distinct chains · 7% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HOmalizumab Fab Ser81Arg, Gln83Arg and Leu158Pro light chain mutantprotein2128% helix, 54% strand—
LOmalizumab Fab Ser81Arg, Gln83Arg and Leu158Pro light chain mutantprotein2166% helix, 53% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 8 copies · chains H, L
  • PEG · Di(hydroxyethyl)ether · additive · chains 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15940.610.7356EDO
2640.530.8722empty
3540.340.7818empty

Interfaces

1 interface between chains.

  • H–L · 1787 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 6TCR · Crystal structure of the omalizumab Fab SER81ARG, GLN83ARG and LEU158PRO light chain… · the same entry in another collection · chain H against H, TM-score 1.00

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