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Crystal structure of human CD38 extracellular domain, ara-F-ribose-5'- PHOSPHATE/NICOTINAMIDE complex

Analyse Crystal structure of human CD38 extracellular domain, ara-F-ribose-5'… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3DZG
Type
protein
Length
504 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ADP-ribosyl cyclase 1
EC
3.2.2.5
UniProt
P28907
Ligands
RF5, NCA
Pockets
5 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BADP-ribosyl cyclase 1 (EC 3.2.2.5)protein25244% helix, 16% strandP28907

Ligands and binding sites

  • RF5 · 2-deoxy-2-fluoro-5-O-phosphono-alpha-D-arabinofuranose · ligand · 2 copies · chains A, B
  • NCA · Nicotinamide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16790.700.7871RF5, NCA
26390.680.7775RF5, NCA
3720.570.8819empty
41070.530.8216empty
51020.370.7415empty

Interfaces

1 interface between chains.

  • A–B · 600 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide, 2 covalent (disulfide, covalent ligand).

Compared structures

  • 3DZG · Crystal structure of human CD38 extracellular domain… · the same entry in another collection · chain A against A, TM-score 1.00
  • P28907 · AlphaFold monomer V2.0 prediction for ADP-ribosyl CYCLASE/CYCLIC ADP- ribose hydrolase 1… · a predicted model of the same protein · chain B against A, TM-score 0.98

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