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Structure of the Fab fragment of N62, a protective monoclonal antibody to the nonreducing end of francisella tularensis O-antigen

Analyse Structure of the Fab fragment of N62, a protective monoclonal antibody to the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4KPH
Type
protein
Length
810 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
N62 light chain; N62 heavy chain
Pockets
7 · best druggability 0.71

Structure

x-ray diffraction · 4 distinct chains · 5% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LN62 light chainprotein2106% helix, 51% strand—
HN62 heavy chainprotein2066% helix, 55% strand—
MN62 light chainprotein1964% helix, 51% strand—
IN62 heavy chainprotein1985% helix, 57% strand—

Ligands and binding sites

  • ACT · Acetate ion · additive · chains M, I

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

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19770.710.7688empty
22900.620.8044empty
32030.590.8126empty
41590.590.8333empty
5520.410.8212empty

Interfaces

5 interfaces between chains.

  • M–I · 1752 Ų buried · 17 hydrogen bonds · protein-protein
  • L–H · 1744 Ų buried · 15 hydrogen bonds · protein-protein
  • L–I · 227 Ų buried · 6 hydrogen bonds · protein-protein
  • H–I · 79 Ų buried · 1 hydrogen bond · protein-protein
  • H–M · 47 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 4 modified (disulfide, cyclization, oxidation).

Compared structures

  • 4KPH · Structure of the Fab fragment of N62, a protective monoclonal antibody to the nonreducing… · the same entry in another collection · chain L against L, TM-score 1.00

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