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PR3 (myeloblastin)

Analyse PR3 (myeloblastin) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FUJ
Type
protein
Length
884 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
PR3
UniProt
P24158
Ligands
NAG, FUC
Pockets
5 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 9% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DPR3protein2219% helix, 38% strandP24158

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B, C, D
  • FUC · alpha-L-fucopyranose · sugar · 4 copies · chains A, B, 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110120.840.8489empty
29710.830.8490empty
3870.350.7519empty
4560.280.7422empty
5500.250.7318empty

Interfaces

4 interfaces between chains.

  • C–D · 792 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 715 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 492 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 391 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 1FUJ · PR3 (myeloblastin) · the same entry in another collection · chain B against B, TM-score 1.00
  • P24158 · AlphaFold monomer V2.0 prediction for myeloblastin (P24158) · a predicted model of the same protein · chain A against A, TM-score 0.99

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