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The structure of dihydropteroate synthase from staphylococcus aureus subsp. aureus MU50.

Analyse The structure of dihydropteroate synthase from staphylococcus aureus subsp.… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4HB7
Type
protein
Length
506 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydropteroate synthase
EC
2.5.1.15
UniProt
P64141
Pockets
2 · best druggability 0.56

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDihydropteroate synthase (EC 2.5.1.15)protein25349% helix, 15% strandP64141

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 7 copies · chains A, B

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

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12600.560.7837empty
21760.550.8030empty

Interfaces

1 interface between chains.

  • A–B · 1598 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 4HB7 · The Structure of Dihydropteroate Synthase from Staphylococcus aureus subsp. aureus Mu50. · the same entry in another collection · chain A against A, TM-score 1.00
  • P64141 · AlphaFold monomer V2.0 prediction for dihydropteroate synthase (P64141) · a predicted model of the same protein · chain A against A, TM-score 0.98

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