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Toxin-Antitoxin complex GraTA

Analyse Toxin-Antitoxin complex GraTA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6F8S
Type
protein
Length
320 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.5
Source
Pseudomonas putida; Pseudomonas putida (strain ATCC 47054 / DSM 6125 / NCIMB…
Molecule
XRE family transcriptional regulator; Putative Killer protein
UniProt
A0A179R2V1, Q88MI5
Ligands
SO4
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · resolution 2.5 · 4 distinct chains · 54% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AXRE family transcriptional regulatorprotein9471% helix, 0% strandA0A179R2V1
BPutative Killer proteinprotein6632% helix, 32% strandQ88MI5
CXRE family transcriptional regulatorprotein9567% helix, 0% strandA0A179R2V1
DPutative Killer proteinprotein6534% helix, 26% strandQ88MI5

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 2 copies · chains A, C
  • PEG · Di(hydroxyethyl)ether · additive · 3 copies · chains B, D, C

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
16110.650.7552PEG
2660.360.7714empty

Interfaces

6 interfaces between chains.

  • A–C · 1516 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 801 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 773 Ų buried · 13 hydrogen bonds · protein-protein
  • B–D · 77 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 53 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6F8S · Toxin-antitoxin complex grata · the same entry in another collection · chain A against A, TM-score 1.00

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