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ADP ribose pyrophosphatase from thermus thermophilus HB8 in esm-state at reaction time of 3 min

Analyse ADP ribose pyrophosphatase from thermus thermophilus HB8 in esm-state at… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3X0M
Type
protein
Length
156 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ADP-ribose pyrophosphatase
EC
3.6.1.13
UniProt
Q5SKW5
Ligands
AR6, MN, SO4
Pockets
1 · best druggability 0.45

Structure

x-ray diffraction · 1 distinct chain · 22% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AADP-ribose pyrophosphatase (EC 3.6.1.13)protein15622% helix, 43% strandQ5SKW5

Ligands and binding sites

  • AR6 · [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methyl [hydroxy-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxolan-2-yl]methoxy]phosphoryl] hydrogen phosphate · ligand · chains A
  • MN · Manganese (II) ion · metal · chains A
  • SO4 · Sulfate ion · ion · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11900.450.7422MN

Compared structures

  • 3X0M · ADP ribose pyrophosphatase from Thermus thermophilus HB8 in ESM-state at reaction time of… · the same entry in another collection · chain A against A, TM-score 1.00

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