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Crystal structure of rabbit muscle glycogen phosphorylase in complex with 3,4-dihydro-2-quinolone

Analyse Crystal structure of rabbit muscle glycogen phosphorylase in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2IEI
Type
protein
Length
1,590 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycogen phosphorylase, muscle form
EC
2.4.1.1
UniProt
P00489
Ligands
PLR, FRX
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 2 distinct chains · 53% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlycogen phosphorylase, muscle form (EC 2.4.1.1)protein79454% helix, 15% strandP00489
BGlycogen phosphorylase, muscle form (EC 2.4.1.1)protein79653% helix, 16% strandP00489

Ligands and binding sites

  • PLR · (5-hydroxy-4,6-dimethylpyridin-3-yl)methyl dihydrogen phosphate · ligand · 2 copies · chains A, B
  • FRX · (S)-2-chloro-N-(1-(2-(2-hydroxyethylamino)-2-oxoethyl)-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)-6H-thieno[2,3-b]pyrrole-5-carboxamide · ligand · 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, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110320.860.8788FRX
22590.830.9549PLR
33580.820.9266PLR
41330.770.9539empty
51180.770.9638empty

Interfaces

1 interface between chains.

  • A–B · 2050 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 2IEI · Crystal structure of rabbit muscle glycogen phosphorylase in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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