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Solution structure of a phage-derived peptide antagonist in complex with vascular endothelial growth factor

Analyse Solution structure of a phage-derived peptide antagonist in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1KAT
Type
protein
Length
236 residues
Chains
4
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Vascular endothelial growth factor; Phage-derived peptide antagonist
UniProt
P15692
Pockets
3 · best druggability 0.42

Structure

solution nmr · 2 distinct chains · 14% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
V, WVascular endothelial growth factorprotein9912% helix, 54% strandP15692
X, YPhage-derived peptide antagonistprotein1926% helix, 0% strand—

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11110.420.7723empty
2810.350.7617empty
3760.310.7416empty

Interfaces

5 interfaces between chains.

  • V–W · 1516 Ų buried · 8 hydrogen bonds · protein-protein
  • W–X · 434 Ų buried · 5 hydrogen bonds · protein-protein
  • V–Y · 423 Ų buried · 3 hydrogen bonds · protein-protein
  • W–Y · 155 Ų buried · 2 hydrogen bonds · protein-protein
  • V–X · 151 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • 1KAT · Solution Structure of a Phage-Derived Peptide Antagonist in Complex with Vascular… · the same entry in another collection · chain V against V, TM-score 1.00
  • P15692 · AlphaFold monomer V2.0 prediction for vascular endothelial growth factor a (P15692) · a predicted model of the same protein · chain V against A, TM-score 0.95

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