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Crystal structure of birch pollen allergen bet V 1 mutant G26L, D69I, P90L, K97I

Analyse Crystal structure of birch pollen allergen bet V 1 mutant G26L, D69I, P90L, K97I in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Z3L
Type
protein
Length
954 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Major pollen allergen bet V 1-a
UniProt
P15494
Ligands
SO4
Pockets
13 · best druggability 0.87

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, E, F, DMajor pollen allergen bet V 1-aprotein15926% helix, 40% strandP15494

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 14 copies · chains A, B, E, C, F

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

Pockets

13 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111920.870.8796SO4
25470.840.8945empty
35290.820.8853empty
44810.820.8845SO4
54700.820.8842empty

Interfaces

6 interfaces between chains.

  • B–C · 678 Ų buried · 18 hydrogen bonds · protein-protein
  • E–F · 667 Ų buried · 17 hydrogen bonds · protein-protein
  • C–D · 635 Ų buried · 5 hydrogen bonds · protein-protein
  • B–E · 444 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 366 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4Z3L · Crystal structure of birch pollen allergen bet V 1 mutant G26L, D69I, P90L, K97I · the same entry in another collection · chain D against D, 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 C against A, TM-score 0.98

Analyse

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