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Orthorhombic form of IGG1 Fab fragment (in complex with antigenic tubulin peptide) sharing same fv as IgA

Analyse Orthorhombic form of IGG1 Fab fragment (in complex with antigenic tubulin… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3QNZ
Type
protein
Length
430 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab fragment of immunoglobulin G1 light chain; Fab fragment of immunoglobulin G1 heavy…
UniProt
P07437
Pockets
3 · best druggability 0.65

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab fragment of immunoglobulin G1 light chainprotein2196% helix, 50% strand—
BFab fragment of immunoglobulin G1 heavy chainprotein20810% helix, 51% strand—
CPeptide from tubulin beta chainprotein30% helix, 0% strandP07437

Ligands and binding sites

  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16480.650.7571empty
21550.430.7423empty
3810.330.7519empty

Interfaces

3 interfaces between chains.

  • A–B · 1508 Ų buried · 16 hydrogen bonds · protein-protein
  • B–C · 171 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 160 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 3QNZ · Orthorhombic form of IgG1 Fab fragment (in complex with antigenic tubulin peptide)… · the same entry in another collection · chain A against A, TM-score 1.00
  • P07437 · AlphaFold monomer V2.0 prediction for tubulin beta chain (P07437) · a predicted model of the same protein · chain C against A, TM-score 1.00

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