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Crystal structure of human 4E10 Fab crystalized in the presence of phosphatidylcholine (06:0 pc); C2 space group

Analyse Crystal structure of human 4E10 Fab crystalized in the presence of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XCE
Type
protein
Length
1,312 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
4E10 Fab light chain; 4E10 Fab heavy chain
Pockets
15 · best druggability 0.81

Structure

x-ray diffraction · 5 distinct chains · 6% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L4E10 Fab light chainprotein2125% helix, 50% strand—
H4E10 Fab heavy chainprotein2237% helix, 52% strand—
B, D4E10 Fab light chainprotein2147% helix, 50% strand—
A4E10 Fab heavy chainprotein2257% helix, 51% strand—
C4E10 Fab heavy chainprotein2245% helix, 50% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110490.810.82107empty
25590.630.7566empty
34730.590.7452empty
44140.560.7455empty
51270.550.8336empty

Interfaces

9 interfaces between chains.

  • D–C · 1614 Ų buried · 11 hydrogen bonds · protein-protein
  • B–A · 1584 Ų buried · 7 hydrogen bonds · protein-protein
  • L–H · 1435 Ų buried · 6 hydrogen bonds · protein-protein
  • H–C · 260 Ų buried · 3 hydrogen bonds · protein-protein
  • H–A · 250 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide (disulfide).

Compared structures

  • 4XCE · Crystal structure of human 4E10 Fab crystalized in the presence of Phosphatidylcholine… · the same entry in another collection · chain L against L, TM-score 1.00

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