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Crystal structure of LI33 IGG2 di-Fab

Analyse Crystal structure of LI33 IGG2 di-Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3KYM
Type
protein
Length
3,449 residues
Chains
16
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Light chain LI33 IGG2; Heavy chain LI33 IGG2
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 5 distinct chains · 5% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, G, I, OLight chain LI33 IGG2protein2136% helix, 50% strand—
B, DHeavy chain LI33 IGG2protein2206% helix, 47% strand—
F, H, J, L, N, PHeavy chain LI33 IGG2protein2197% helix, 52% strand—
KLight chain LI33 IGG2protein2093% helix, 36% strand—
MLight chain LI33 IGG2protein2082% helix, 45% strand—

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111030.870.88110empty
21130.750.9531empty
310940.750.78126empty
47270.720.7888empty
52210.640.8231empty

Interfaces

31 interfaces between chains.

  • O–P · 1849 Ų buried · 13 hydrogen bonds · protein-protein
  • E–F · 1825 Ų buried · 11 hydrogen bonds · protein-protein
  • I–J · 1811 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 1789 Ų buried · 13 hydrogen bonds · protein-protein
  • C–D · 1775 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 disulfide (disulfide).

Compared structures

  • 3KYM · Crystal structure of Li33 IgG2 di-Fab · the same entry in another collection · chain A against A, TM-score 1.00

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