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Structural and mechanistic changes along an engineered path from metallo to non-metallo KDO8P synthase

Analyse Structural and mechanistic changes along an engineered path from metallo to… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2NWS
Type
protein
Length
525 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-dehydro-3-deoxyphosphooctonate aldolase
EC
2.5.1.55
UniProt
O66496
Ligands
PEP, A5P
Pockets
5 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A2-dehydro-3-deoxyphosphooctonate aldolase (EC 2.5.1.55)protein26341% helix, 21% strandO66496
B2-dehydro-3-deoxyphosphooctonate aldolase (EC 2.5.1.55)protein26242% helix, 19% strandO66496

Ligands and binding sites

  • PEP · Phosphoenolpyruvate · ligand · 2 copies · chains A, B
  • A5P · Arabinose-5-phosphate · ligand · 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
11720.800.9547PEP, A5P
21840.780.9445PEP, A5P
3930.550.8531empty
41050.420.7721empty
5560.300.7512empty

Interfaces

1 interface between chains.

  • A–B · 1927 Ų buried · 30 hydrogen bonds · protein-protein

Compared structures

  • 2NWS · Structural and mechanistic changes along an engineered path from metallo to non-metallo… · the same entry in another collection · chain A against A, TM-score 1.00

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