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Crystal structure of folp (dihydropteroate synthase) from colstridium difficile in the presence of pteroic acid

Analyse Crystal structure of folp (dihydropteroate synthase) from colstridium difficile… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6PZ2
Type
protein
Length
263 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydropteroate synthase
EC
2.5.1.15
UniProt
A0A160WS51
Ligands
PT1, SO4
Pockets
4 · best druggability 0.61

Structure

x-ray diffraction · 1 distinct chain · 48% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydropteroate synthase (EC 2.5.1.15)protein26348% helix, 14% strandA0A160WS51

Ligands and binding sites

  • PT1 · Pteroic acid · ligand · chains A
  • SO4 · Sulfate ion · ion · 9 copies · chains A
  • NHE · 2-[N-cyclohexylamino]ethane sulfonic acid · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12260.610.8138SO4, PT1
2890.360.7517SO4
3610.330.7616NHE
4670.330.7515empty

Compared structures

  • 6PZ2 · Crystal Structure of FolP (dihydropteroate synthase) from Colstridium difficile in the… · the same entry in another collection · chain A against A, TM-score 1.00

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