GL1X · GenesisL1 explorer

Research workbench

Phosphopentomutase S154A variant

Analyse Phosphopentomutase S154A variant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4LR7
Type
protein
Length
1,171 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphopentomutase
EC
5.4.2.7
UniProt
Q818Z9
Ligands
MN
Pockets
6 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhosphopentomutase (EC 5.4.2.7)protein39135% helix, 21% strandQ818Z9
B, CPhosphopentomutase (EC 5.4.2.7)protein39036% helix, 21% strandQ818Z9

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 14 copies · chains A, B, C
  • GOL · Glycerol · additive · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111420.800.82110MN
29920.780.8093GOL
3540.370.8014empty
4880.320.7322empty
5580.310.7615empty

Interfaces

2 interfaces between chains.

  • B–C · 936 Ų buried · 24 hydrogen bonds · protein-protein
  • A–B · 325 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (phosphorylation).

Compared structures

  • 4LR7 · Phosphopentomutase S154A variant · the same entry in another collection · chain A against A, TM-score 1.00
  • Q818Z9 · AlphaFold monomer V2.0 prediction for phosphopentomutase (Q818Z9) · a predicted model of the same protein · chain A against A, TM-score 0.99

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.