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MolNFT v1 · #76540 · protein

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

3QNZ · Fab fragment of immunoglobulin G1 light chain: “Orthorhombic form of IGG1 Fab fragment (in complex with antigenic tubulin peptide) sharing same fv as IgA”. X-ray diffraction, 3 pockets (best druggability 0.65). MolNFT v1 #76540 on…

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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