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Phosphorylase recognition and phosphorolysis of its oligosaccharide substrate: answers to a long outstanding question

Analyse Phosphorylase recognition and phosphorolysis of its oligosaccharide substrate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1E4O
Type
protein
Length
1,592 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Maltodextrin phosphorylase
EC
2.4.1.1
UniProt
P00490
Ligands
PLP, GLC, BGC
Pockets
19 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 53% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BMaltodextrin phosphorylase (EC 2.4.1.1)protein79653% helix, 11% strandP00490

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • GLC · alpha-D-glucopyranose · sugar · 8 copies · chains A, B
  • BGC · beta-D-glucopyranose · sugar · 2 copies · chains A, B

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

Pockets

19 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110750.840.8581empty
27060.820.8686BGC, GLC, PLP
37140.810.8588BGC, GLC, PLP
45120.670.7852empty
54800.650.7854empty

Interfaces

1 interface between chains.

  • A–B · 2083 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 1E4O · Phosphorylase recognition and phosphorolysis of its oligosaccharide substrate: answers to… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00490 · AlphaFold monomer V2.0 prediction for maltodextrin phosphorylase (P00490) · a predicted model of the same protein · chain A against A, TM-score 1.00

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