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Crystal structure of a unusually linked dimeric variant of bet V 1

Analyse Crystal structure of a unusually linked dimeric variant of bet V 1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4BKC
Type
protein
Length
318 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Major pollen allergen bet V 1-a
UniProt
P15494
Pockets
2 · best druggability 0.88

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BMajor pollen allergen bet V 1-aprotein15926% helix, 40% strandP15494

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111210.880.88111empty
2530.260.7314empty

Interfaces

1 interface between chains.

  • A–B · 676 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (nonstandard).

Compared structures

  • 4BKC · Crystal Structure of a unusually linked dimeric variant of Bet v 1 · the same entry in another collection · chain A against A, TM-score 1.00
  • P15494 · AlphaFold monomer V2.0 prediction for major pollen allergen bet V 1-a (P15494) · a predicted model of the same protein · chain B against A, TM-score 0.98

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