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Lyme disease antigen ospa in complex with neutralizing antibody Fab la-2

Analyse Lyme disease antigen ospa in complex with neutralizing antibody Fab la-2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FJ1
Type
protein
Length
1,354 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hybridoma antibody LA2 (light chain); Hybridoma antibody LA2 (heavy chain); Outer surface…
UniProt
P14013
Pockets
17 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHybridoma antibody LA2 (light chain)protein2137% helix, 52% strand—
B, DHybridoma antibody LA2 (heavy chain)protein2137% helix, 53% strand—
E, FOuter surface protein aprotein2513% helix, 45% strandP14013

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16890.810.86109empty
24190.670.8038empty
34820.650.7732empty
41670.560.8122empty
51180.550.8326empty

Interfaces

12 interfaces between chains.

  • A–B · 1848 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 1809 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 1056 Ų buried · 9 hydrogen bonds · protein-protein
  • C–E · 499 Ų buried · 5 hydrogen bonds · protein-protein
  • A–F · 482 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 1FJ1 · Lyme disease antigen ospa in complex with neutralizing antibody Fab la-2 · the same entry in another collection · chain D against D, TM-score 1.00

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