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Crystal structure of kdo-8-phosphate synthase

Analyse Crystal structure of kdo-8-phosphate synthase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1O60
Type
protein
Length
1,076 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-dehydro-3-deoxyphosphooctonate aldolase
EC
2.5.1.55
UniProt
P45251
Pockets
14 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D2-dehydro-3-deoxyphosphooctonate aldolase (EC 2.5.1.55)protein26942% helix, 21% strandP45251

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15790.760.8349empty
25800.740.8153empty
36110.740.8151empty
45750.730.8148empty
51410.670.8830empty

Interfaces

6 interfaces between chains.

  • A–C · 1580 Ų buried · 28 hydrogen bonds · protein-protein
  • A–B · 1578 Ų buried · 12 hydrogen bonds · protein-protein
  • C–D · 1483 Ų buried · 13 hydrogen bonds · protein-protein
  • B–D · 1477 Ų buried · 24 hydrogen bonds · protein-protein
  • B–C · 214 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 36 modified (engineered).

Compared structures

  • 1O60 · Crystal structure of KDO-8-phosphate synthase · the same entry in another collection · chain B against B, TM-score 1.00
  • P45251 · AlphaFold monomer V2.0 prediction for 2-dehydro-3-deoxyphosphooctonate aldolase (P45251) · a predicted model of the same protein · chain A against A, TM-score 0.99

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