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MolNFT v1 · #78240 · protein

Structural basis for the function of two anti-VEGF receptor antibodies

3S35 · 6.64 Fab heavy chain: “Structural basis for the function of two anti-VEGF receptor antibodies”. X-ray diffraction, 2 ligands (NAG, CA), 6 pockets (best druggability 0.67). MolNFT v1 #78240 on GenesisL1: 3D structure, binding sites…

PDB
3S35
Type
protein
Length
540 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
6.64 Fab heavy chain; 6.64 Fab light chain; Vascular endothelial growth factor receptor 2
EC
2.7.10.1
UniProt
P35968
Ligands
NAG, CA
Pockets
6 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 54% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H6.64 Fab heavy chainprotein2117% helix, 54% strand—
L6.64 Fab light chainprotein2176% helix, 52% strand—
XVascular endothelial growth factor receptor 2 (EC 2.7.10.1)protein1126% helix, 56% strandP35968

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 3 copies · chains L, X
  • CA · Calcium ion · metal · 6 copies · chains H, X, L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11030.670.9130CA
21910.490.7639empty
3610.360.7919empty
4910.340.7417empty
5580.290.7415empty

Interfaces

3 interfaces between chains.

  • H–L · 1673 Ų buried · 12 hydrogen bonds · protein-protein
  • H–X · 692 Ų buried · 11 hydrogen bonds · protein-protein
  • L–X · 514 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 3S35 · Structural basis for the function of two anti-VEGF receptor antibodies · the same entry in another collection · chain H against H, TM-score 1.00

Analyse

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