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Crystal structure of plasmodium falciparum hppk-dhps wild type

Analyse Crystal structure of plasmodium falciparum hppk-dhps wild type in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JWQ
Type
protein
Length
1,138 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
7,8-dihydro-6-hydroxymethylpterin pyrophosphokinase- dihydropteroate synthase
UniProt
Q25704
Ligands
ATP, AMP, MG, CA
Pockets
20 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A7,8-dihydro-6-hydroxymethylpterin pyrophosphokinase- dihydropteroate synthaseprotein54844% helix, 16% strandQ25704
B7,8-dihydro-6-hydroxymethylpterin pyrophosphokinase- dihydropteroate synthaseprotein59044% helix, 16% strandQ25704

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · chains A
  • AMP · Adenosine monophosphate · ligand · chains B
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • CA · Calcium ion · metal · chains A
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17230.710.7873empty
25030.650.7758MG, ATP
33880.620.7741AMP, MG
43700.580.7645empty
52100.580.8038empty

Interfaces

1 interface between chains.

  • A–B · 1765 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 6JWQ · Crystal structure of Plasmodium falciparum HPPK-DHPS wild type · the same entry in another collection · chain A against A, TM-score 1.00

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