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The catalytic domain of gdpp with C-di-AMP

Analyse The catalytic domain of gdpp with C-di-AMP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XSN
Type
protein
Length
666 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphodiesterase acting on cyclic dinucleotides
UniProt
A0A0U1MUE2
Ligands
2BA, MN
Pockets
2 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 45% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPhosphodiesterase acting on cyclic dinucleotidesprotein33345% helix, 19% strandA0A0U1MUE2

Ligands and binding sites

  • 2BA · (2r,3r,3as,5r,7ar,9r,10r,10as,12r,14ar)-2,9-bis(6-amino-9H-purin-9-yl)octahydro-2H,7H-difuro[3,2-D:3', 2'-J][1,3,7,9,2,8 ]tetraoxadiphosphacyclododecine-3,5, 10,12-tetrol 5,12-dioxide · ligand · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 4 copies · chains A, B

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
110860.750.7862empty
2510.270.7514empty

Interfaces

1 interface between chains.

  • A–B · 1641 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 5XSN · The catalytic domain of GdpP with c-di-AMP · the same entry in another collection · chain A against A, TM-score 1.00

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