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Schistosoma haematobium (blood fluke) sulfotransferase

Analyse Schistosoma haematobium (blood fluke) sulfotransferase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TIV
Type
protein
Length
246 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sulfotransferase
UniProt
A0A094ZWQ2
Ligands
A3P
Pockets
1 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 57% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASulfotransferaseprotein24657% helix, 7% strandA0A094ZWQ2

Ligands and binding sites

  • A3P · Adenosine-3'-5'-diphosphate · ligand · chains A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13030.750.8758A3P, TRS

Compared structures

  • 5TIV · Schistosoma haematobium (Blood Fluke) Sulfotransferase · the same entry in another collection · chain A against A, TM-score 1.00

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