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Crystal structure of der P 1 complexed with Fab 4C1

Analyse Crystal structure of der P 1 complexed with Fab 4C1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5VPG
Type
protein
Length
651 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Der P 1 allergen; Fab 4C1 - light chain; Fab 4C1 - heavy chain
UniProt
Q3HWZ5
Ligands
NAG, CA
Pockets
5 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 13% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADer P 1 allergenprotein22228% helix, 25% strandQ3HWZ5
CFab 4C1 - light chainprotein2116% helix, 54% strand—
DFab 4C1 - heavy chainprotein2186% helix, 51% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains A
  • CA · Calcium ion · metal · chains A
  • EDO · 1,2-ethanediol · additive · 8 copies · chains A, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15230.610.7455empty
22610.600.7937EDO
3560.500.8720empty
41510.420.7425empty
51060.360.7426empty

Interfaces

3 interfaces between chains.

  • C–D · 2015 Ų buried · 26 hydrogen bonds · protein-protein
  • A–D · 617 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 216 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 5VPG · Crystal structure of der P 1 complexed with Fab 4C1 · the same entry in another collection · chain A against A, TM-score 1.00

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