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

Analyse Phosphorylase recognition and phosphorylysis 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
1QM5
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
SGC, PLP, GLC, PO4
Pockets
20 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 54% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BMaltodextrin phosphorylase (EC 2.4.1.1)protein79654% helix, 13% strandP00490

Ligands and binding sites

  • SGC · 4-thio-beta-D-glucopyranose · ligand · 2 copies · chains A, B
  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • GLC · alpha-D-glucopyranose · sugar · 8 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110520.840.8573empty
27020.820.8685GLC, SGC, PO4, PLP
36660.810.8683GLC, SGC, PO4, PLP
4630.740.9917empty
5540.730.9917empty

Interfaces

1 interface between chains.

  • A–B · 2149 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 1QM5 · Phosphorylase recognition and phosphorylysis 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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