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Crystal structure of a lewis-binding Fab (CH88.2)

Analyse Crystal structure of a lewis-binding Fab (CH88.2) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6X5E
Type
protein
Length
867 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CH88.2 Fab light chain; CH88.2 Fab heavy chain
Ligands
NI
Pockets
8 · best druggability 0.58

Structure

x-ray diffraction · 4 distinct chains · 4% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LCH88.2 Fab light chainprotein2134% helix, 49% strand—
HCH88.2 Fab heavy chainprotein2193% helix, 53% strand—
ACH88.2 Fab light chainprotein2145% helix, 50% strand—
BCH88.2 Fab heavy chainprotein2215% helix, 51% strand—

Ligands and binding sites

  • NI · Nickel (II) ion · metal · 3 copies · chains L, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13980.580.7549empty
24510.580.7461empty
32950.570.7740empty
4710.480.8426empty
51450.460.7724empty

Interfaces

4 interfaces between chains.

  • A–B · 1792 Ų buried · 17 hydrogen bonds · protein-protein
  • L–H · 1712 Ų buried · 12 hydrogen bonds · protein-protein
  • L–A · 223 Ų buried · 3 hydrogen bonds · protein-protein
  • H–A · 52 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6X5E · Crystal structure of a Lewis-binding Fab (ch88.2) · the same entry in another collection · chain L against L, TM-score 1.00

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