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Fab fragment (MN14C11.6) in complex with a peptide antigen derived from neisseria meningitidis P1.7 serosubtype antigen and domain II from streptococcal protein G

Analyse Fab fragment (MN14C11.6) in complex with a peptide antigen derived from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QKZ
Type
protein
Length
501 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein G-prime; Antibody; Major outer membrane protein P1.16
UniProt
Q54181, Q06140
Pockets
6 · best druggability 0.56

Structure

x-ray diffraction · 4 distinct chains · 8% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein G-primeprotein5824% helix, 47% strandQ54181
HAntibodyprotein2195% helix, 47% strand—
LAntibodyprotein2146% helix, 52% strand—
PMajor outer membrane protein P1.16protein100% helix, 20% strandQ06140

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13680.560.7545empty
21460.470.7736empty
31660.450.7524empty
41170.410.7625empty
5580.310.7514empty

Interfaces

5 interfaces between chains.

  • H–L · 1874 Ų buried · 15 hydrogen bonds · protein-protein
  • A–H · 565 Ų buried · 13 hydrogen bonds · protein-protein
  • H–P · 493 Ų buried · 5 hydrogen bonds · protein-protein
  • L–P · 169 Ų buried · 1 hydrogen bond · protein-protein
  • A–L · 140 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 1QKZ · Fab fragment (MN14C11.6) in complex with a peptide antigen derived from Neisseria… · the same entry in another collection · chain A against A, TM-score 1.00

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