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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 v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Xre family transcriptional regulator; Putative killer protein
UniProt
A0A179R2V1, Q88MI5
Ligands
SO4
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · 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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