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ADP-ribosylserine hydrolase ARH3 of latimeria chalumnae in complex with ADP-hpm

Analyse ADP-ribosylserine hydrolase ARH3 of latimeria chalumnae in complex with ADP-hpm in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6HH5
Type
protein
Length
655 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ADP-ribosylhydrolase like 2
UniProt
H3BCW1
Ligands
A3R, MG
Pockets
4 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 68% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AADP-ribosylhydrolase like 2protein32768% helix, 2% strandH3BCW1
BADP-ribosylhydrolase like 2protein32867% helix, 2% strandH3BCW1

Ligands and binding sites

  • A3R · Adenosine Diphosphate (Hydroxymethyl)pyrrolidine monoalcohol · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19800.870.88106A3R
2910.440.7923empty
3700.340.7617empty
4710.340.7617GOL

Interfaces

1 interface between chains.

  • A–B · 756 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 6HH5 · ADP-ribosylserine hydrolase ARH3 of Latimeria chalumnae in complex with ADP-HPM · the same entry in another collection · chain A against A, TM-score 1.00
  • H3BCW1 · AlphaFold monomer V2.0 prediction for ADP-ribose glycohydrolase ARH3 (H3BCW1) · a predicted model of the same protein · chain B against A, TM-score 0.99

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