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Crystal structure of the kiwifruit allergen act D 5

Analyse Crystal structure of the kiwifruit allergen act D 5 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4X9U
Type
protein
Length
326 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kiwellin
UniProt
P84527
Pockets
3 · best druggability 0.51

Structure

x-ray diffraction · 2 distinct chains · 12% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKiwellinprotein18310% helix, 27% strandP84527
BKiwellinprotein14313% helix, 35% strandP84527

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12190.510.7624empty
22180.480.7525empty
31050.340.7323empty

Interfaces

1 interface between chains.

  • A–B · 276 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 11 disulfide, 1 modified (disulfide, nonstandard).

Compared structures

  • 4X9U · Crystal structure of the kiwifruit allergen Act d 5 · the same entry in another collection · chain A against A, TM-score 1.00
  • P84527 · AlphaFold monomer V2.0 prediction for kiwellin (P84527) · a predicted model of the same protein · chain B against A, TM-score 0.99

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