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Structure of the B20-4 Fab, a phage derived Fab fragment, in complex with VEGF

Analyse Structure of the B20-4 Fab, a phage derived Fab fragment, in complex with VEGF in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2FJH
Type
protein
Length
1,058 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Vascular endothelial growth factor a; Fab fragment light chain; Fab fragment heavy chain
UniProt
Q96NW5
Pockets
9 · best druggability 0.75

Structure

x-ray diffraction · 5 distinct chains · 8% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
VVascular endothelial growth factor aprotein9812% helix, 58% strandQ96NW5
LFab fragment light chainprotein2147% helix, 50% strand—
H, BFab fragment heavy chainprotein2197% helix, 51% strand—
WVascular endothelial growth factor aprotein9712% helix, 57% strandQ96NW5
AFab fragment light chainprotein2115% helix, 50% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110280.750.7899empty
21600.630.8536empty
35910.620.7454empty
44840.580.7353empty
51770.460.7531empty

Interfaces

8 interfaces between chains.

  • L–H · 1777 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 1714 Ų buried · 15 hydrogen bonds · protein-protein
  • V–H · 554 Ų buried · 3 hydrogen bonds · protein-protein
  • W–B · 519 Ų buried · 3 hydrogen bonds · protein-protein
  • V–L · 372 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 disulfide (disulfide).

Compared structures

  • 2FJH · Structure of the B20-4 Fab, a phage derived Fab fragment, in complex with VEGF · the same entry in another collection · chain V against V, TM-score 1.00

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