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Thiosulfate dehydrogenase (tsdba) from marichromatium purpuratum - "as isolated" form

Analyse Thiosulfate dehydrogenase (tsdba) from marichromatium purpuratum - "as… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LO9
Type
protein
Length
940 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cytochrome C
UniProt
W0DW89
Ligands
HEC, THJ, CL
Pockets
11 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACytochrome Cprotein47144% helix, 5% strandW0DW89
BCytochrome Cprotein46943% helix, 5% strandW0DW89

Ligands and binding sites

  • HEC · Heme C · ligand · 8 copies · chains A, B
  • THJ · Thiosulfate · ligand · 2 copies · chains A, B
  • CL · Chloride ion · ion · 11 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 12 copies · chains A, B
  • PGO · S-1,2-propanediol · additive · 4 copies · chains A, B
  • PGE · Triethylene glycol · additive · chains A

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110470.880.88128HEC, CL, EDO
210850.870.88135HEC, CL
35400.730.8154HEC, THJ
4650.720.9819EDO
55540.720.8052HEC, THJ, EDO

Interfaces

1 interface between chains.

  • A–B · 1145 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 cofactor, 2 covalent (heme c attachment, covalent ligand).

Compared structures

  • 5LO9 · Thiosulfate dehydrogenase (TsdBA) from Marichromatium purpuratum - "as isolated" form · the same entry in another collection · chain A against A, TM-score 1.00

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