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Crystal structure of DAH7PS from neisseria meningitidis

Analyse Crystal structure of DAH7PS from neisseria meningitidis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4HSN
Type
protein
Length
1,364 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3-deoxy-D-arabino-heptulosonate 7-phosphate synthase
EC
2.5.1.54
UniProt
Q9K169
Ligands
PEP, MN, SO4
Pockets
18 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (EC 2.5.1.54)protein34141% helix, 18% strandQ9K169

Ligands and binding sites

  • PEP · Phosphoenolpyruvate · ligand · 4 copies · chains A, B, C, D
  • MN · Manganese (II) ion · metal · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, D

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

Pockets

18 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1550.710.9816empty
2510.700.9816empty
33910.690.8164empty
4500.690.9716empty
52600.690.8440empty

Interfaces

6 interfaces between chains.

  • C–D · 2913 Ų buried · 42 hydrogen bonds · protein-protein
  • A–B · 2810 Ų buried · 40 hydrogen bonds · protein-protein
  • B–D · 559 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 554 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 60 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4HSN · Crystal structure of DAH7PS from Neisseria meningitidis · the same entry in another collection · chain A against A, TM-score 1.00

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