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E. COLI bifunctional glutathionylspermidine SYNTHETASE/AMIDASE incomplex with MG2+ and amppnp

Analyse E. COLI bifunctional glutathionylspermidine SYNTHETASE/AMIDASE incomplex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2IO7
Type
protein
Length
1,174 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional glutathionylspermidine SYNTHETASE/AMIDASE
EC
6.3.1.8, 3.5.1.78
UniProt
P0AES0
Ligands
ANP, MG
Pockets
14 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 26% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional glutathionylspermidine SYNTHETASE/AMIDASE (EC 6.3.1.8, 3.5.1.78)protein58727% helix, 27% strandP0AES0
BBifunctional glutathionylspermidine SYNTHETASE/AMIDASE (EC 6.3.1.8, 3.5.1.78)protein58726% helix, 29% strandP0AES0

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 4 copies · chains A, B

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

Pockets

14 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15970.820.8883MG, ANP
26180.820.8775MG, ANP
36270.760.8245empty
45290.750.8368empty
56010.750.8266empty

Interfaces

1 interface between chains.

  • A–B · 1726 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 2IO7 · E. coli Bifunctional glutathionylspermidine synthetase/amidase Incomplex with Mg2+ and… · the same entry in another collection · chain A against A, TM-score 1.00
  • P0AES0 · AlphaFold monomer V2.0 prediction for bifunctional glutathionylspermidine… · a predicted model of the same protein · chain A against A, TM-score 1.00

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