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MolNFT v2 · #26636 · protein

Crystallographic studies on acyl ureas, a new class of inhibitors of glycogenphosphorylase. Broad specificity of the allosteric site

1WV1 · Glycogen phosphorylase, muscle form: “Crystallographic studies on acyl ureas, a new class of inhibitors of glycogenphosphorylase. Broad specificity…”. X-ray diffraction at 2.26, 2 ligands (PLP, BN5), 13 pockets (best druggability…

PDB
1WV1
Type
protein
Length
816 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.26
Source
Oryctolagus cuniculus
Molecule
Glycogen phosphorylase, muscle form
EC
2.4.1.1
UniProt
P00489
Ligands
PLP, BN5
Pockets
13 · best druggability 0.84

Structure

x-ray diffraction · resolution 2.26 · 1 distinct chain · 52% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlycogen phosphorylase, muscle form (EC 2.4.1.1)protein81652% helix, 15% strandP00489

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · chains A
  • BN5 · 5-[3-({[(2,4-dichlorobenzoyl)amino]carbonyl}amino)-2-methylphenoxy]pentanoic acid · ligand · chains A

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

Pockets

13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12750.840.9650PLP
21400.790.9643empty
32920.690.8432empty
41650.520.7925empty
51130.520.8220empty

Modifications

Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 1WV1 · Crystallographic studies on acyl ureas, a new class of inhibitors of… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00489 · AlphaFold monomer V2.0 prediction for glycogen phosphorylase, muscle form (P00489) · a predicted model of the same protein · chain A against A, TM-score 0.97

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