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Crystal structure of ARC4 from human tankyrase 2 in complex with peptide from human lnpep (chimeric peptide)

Analyse Crystal structure of ARC4 from human tankyrase 2 in complex with peptide from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TWW
Type
protein
Length
337 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tankyrase-2; Human lnpep
EC
2.4.2.30
UniProt
Q9H2K2
Ligands
SO4
Pockets
2 · best druggability 0.74

Structure

x-ray diffraction · 4 distinct chains · 46% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATankyrase-2 (EC 2.4.2.30)protein15750% helix, 0% strandQ9H2K2
BTankyrase-2 (EC 2.4.2.30)protein15749% helix, 0% strandQ9H2K2
CHuman lnpepprotein120% helix, 0% strand—
DHuman lnpepprotein110% helix, 0% strand—

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 2 copies · chains B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13310.740.8543empty
21400.430.7617SO4

Interfaces

6 interfaces between chains.

  • A–C · 712 Ų buried · 11 hydrogen bonds · protein-protein
  • B–D · 678 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 293 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 262 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 239 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (nonstandard).

Compared structures

  • 3TWW · Crystal structure of ARC4 from human Tankyrase 2 in complex with peptide from human LNPEP… · the same entry in another collection · chain A against A, TM-score 1.00

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