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Structure, Function, Stability and Knockout Phenotype of Dihydrodipicolinate Synthase from Streptococcus pneumoniae

Analyse Structure, Function, Stability and Knockout Phenotype of Dihydrodipicolinate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3VFL
Type
protein
Length
614 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.91
Source
Streptococcus pneumoniae
Molecule
Dihydrodipicolinate synthase
EC
4.2.1.52
UniProt
A5LD17
Ligands
K
Pockets
5 · best druggability 0.74

Structure

x-ray diffraction · resolution 1.91 · 2 distinct chains · 48% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydrodipicolinate synthase (EC 4.2.1.52)protein30848% helix, 13% strandA5LD17
BDihydrodipicolinate synthase (EC 4.2.1.52)protein30648% helix, 13% strandA5LD17

Ligands and binding sites

  • K · Potassium ion · metal · 4 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains A, B

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
15910.740.8157K, GOL
21530.530.8030MES
31310.510.8024MES
4870.380.7619empty
5740.360.7717empty

Interfaces

1 interface between chains.

  • A–B · 1975 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 3VFL · Structure, function, stability and knockout phenotype of dihydrodipicolinate synthase… · the same entry in another collection · chain A against A, TM-score 1.00

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