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Structure of the artt motif E214N mutant C3BOT1 exoenzyme (free state, crystal form III)

Analyse Structure of the artt motif E214N mutant C3BOT1 exoenzyme (free state, crystal… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2C8E
Type
protein
Length
596 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mono-ADP-ribosyltransferase C3
EC
2.4.2.-
UniProt
P15879
Ligands
SO4
Pockets
6 · best druggability 0.58

Structure

x-ray diffraction · 3 distinct chains · 34% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
EMono-ADP-ribosyltransferase C3 (EC 2.4.2.-)protein20036% helix, 25% strandP15879
FMono-ADP-ribosyltransferase C3 (EC 2.4.2.-)protein20033% helix, 25% strandP15879
GMono-ADP-ribosyltransferase C3 (EC 2.4.2.-)protein19633% helix, 26% strandP15879

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 4 copies · chains E, F, G

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11870.580.8128SO4
21620.540.8024empty
32300.520.7637SO4
42110.520.7739SO4
52230.460.7422empty

Interfaces

3 interfaces between chains.

  • E–F · 532 Ų buried · 8 hydrogen bonds · protein-protein
  • F–G · 273 Ų buried · 5 hydrogen bonds · protein-protein
  • E–G · 15 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 2C8E · Structure of the ARTT motif E214N mutant C3bot1 Exoenzyme (Free state, crystal form III) · the same entry in another collection · chain E against E, TM-score 1.00

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