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Plasmodium falciparum HSP70-X chaperone nucleotide binding domain in complex with Z396380540

Analyse Plasmodium falciparum HSP70-X chaperone nucleotide binding domain in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7NQU
Type
protein
Length
765 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heat shock protein 70
UniProt
K7NTP5
Ligands
AN2, HR5, CL, PO4
Pockets
5 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHeat shock protein 70protein38639% helix, 28% strandK7NTP5
BHeat shock protein 70protein37941% helix, 28% strandK7NTP5

Ligands and binding sites

  • AN2 · Amp phosphoramidate · ligand · 2 copies · chains A, B
  • HR5 · ~{N}-(cyclobutylmethyl)-1,5-dimethyl-pyrazole-4-carboxamide · ligand · chains B
  • CL · Chloride ion · ion · 3 copies · chains A
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 14 copies · chains A, B
  • PG4 · Tetraethylene glycol · additive · chains A

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16370.790.8472AN2, GOL, PO4
26910.760.8263AN2, GOL, PO4
310450.720.7571CL, HR5, GOL
42090.490.7530GOL
5530.300.7613empty

Interfaces

1 interface between chains.

  • A–B · 517 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (oxidation).

Compared structures

  • 7NQU · Plasmodium falciparum Hsp70-x chaperone nucleotide binding domain in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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