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Crystal structure of the Fab fragment of anti-HER2 antibody 4D5 with redesigned heavy and light chain interfaces

Analyse Crystal structure of the Fab fragment of anti-HER2 antibody 4D5 with redesigned… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TDN
Type
protein
Length
853 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Anti-HER2 Fab light chain; Anti-HER2 Fab heavy chain
Pockets
10 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CAnti-HER2 Fab light chainprotein2136% helix, 50% strand—
BAnti-HER2 Fab heavy chainprotein2148% helix, 51% strand—
DAnti-HER2 Fab heavy chainprotein21312% helix, 54% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · 3 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14930.590.7445empty
22600.560.7735GOL
31910.520.7826empty
42070.450.7329empty
51890.440.7435empty

Interfaces

3 interfaces between chains.

  • A–B · 1793 Ų buried · 12 hydrogen bonds · protein-protein
  • C–D · 1757 Ų buried · 12 hydrogen bonds · protein-protein
  • B–D · 712 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 5TDN · Crystal structure of the Fab fragment of anti-HER2 antibody 4D5 with redesigned heavy and… · the same entry in another collection · chain A against A, TM-score 1.00

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