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Crystal structure of BH1 Fab variant (cdr H3 loop design 16_0325) in complex with VEGF

Analyse Crystal structure of BH1 Fab variant (cdr H3 loop design 16_0325) in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7KEZ
Type
protein
Length
530 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Anti-VEGF-a Fab BH1 heavy chain; Anti-VEGF-a Fab BH1 light chain; Isoform L-VEGF206 of…
Ligands
CL
Pockets
5 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 54% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HAnti-VEGF-a Fab BH1 heavy chainprotein2208% helix, 52% strand—
LAnti-VEGF-a Fab BH1 light chainprotein2166% helix, 52% strand—
VIsoform L-VEGF206 of vascular endothelial growth factor aprotein9413% helix, 61% strand—

Ligands and binding sites

  • CL · Chloride ion · ion · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15890.610.7360empty
21270.420.7624empty
3830.350.7518empty
4970.340.7424empty
5530.300.7614empty

Interfaces

3 interfaces between chains.

  • H–L · 1842 Ų buried · 17 hydrogen bonds · protein-protein
  • L–V · 476 Ų buried · 11 hydrogen bonds · protein-protein
  • H–V · 376 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide (disulfide).

Compared structures

  • 7KEZ · Crystal structure of bH1 Fab variant (CDR H3 loop design 16_0325) in complex with VEGF · the same entry in another collection · chain H against H, TM-score 1.00

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