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Structure of a mutant cetuximab Fab fragment

Analyse Structure of a mutant cetuximab Fab fragment in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ARP
Type
protein
Length
857 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cetuximab mutant light CHAIN,UNCHARACTERIZED protein; Cetuximab mutant Fab heavy…
UniProt
Q8TCD0, P0DOX5
Ligands
SO4
Pockets
8 · best druggability 0.68

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, ACetuximab mutant light CHAIN,UNCHARACTERIZED proteinprotein2136% helix, 51% strandQ8TCD0
DCetuximab mutant Fab heavy CHAIN,IMMUNOGLOBULIN gamma-1 heavy chainprotein2178% helix, 51% strandP0DOX5
BCetuximab mutant Fab heavy CHAIN,IMMUNOGLOBULIN gamma-1 heavy chainprotein2148% helix, 51% strandP0DOX5

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 4 copies · chains C, D, A
  • GOL · Glycerol · additive · 7 copies · chains C, D, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15790.680.7874empty
26690.650.7571empty
35470.630.7556empty
4560.520.8821empty
51500.460.7628empty

Interfaces

3 interfaces between chains.

  • A–B · 1755 Ų buried · 18 hydrogen bonds · protein-protein
  • C–D · 1732 Ų buried · 17 hydrogen bonds · protein-protein
  • C–A · 685 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6ARP · Structure of a mutant Cetuximab Fab fragment · the same entry in another collection · chain C against C, TM-score 1.00

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