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Crystal structure of human ADP-ribose pyrophosphatase NUDT5

Analyse Crystal structure of human ADP-ribose pyrophosphatase NUDT5 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2DSB
Type
protein
Length
824 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ADP-sugar pyrophosphatase
EC
3.6.1.13, 3.6.1.-
UniProt
Q9UKK9
Pockets
8 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 23% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DADP-sugar pyrophosphatase (EC 3.6.1.13, 3.6.1.-)protein20623% helix, 39% strandQ9UKK9

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18780.790.8295empty
24810.740.8343empty
34030.720.8345empty
44110.700.8245empty
53880.680.8142empty

Interfaces

5 interfaces between chains.

  • C–D · 3658 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 3192 Ų buried · 32 hydrogen bonds · protein-protein
  • B–C · 822 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 278 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 174 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 2DSB · Crystal structure of human ADP-ribose pyrophosphatase NUDT5 · the same entry in another collection · chain A against A, TM-score 1.00

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