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Crystal structure of 2-dehydro-3-deoxyphosphogluconate ALDOLASE/4- hydroxy-2-oxoglutarate aldolase (TM0066) from thermotoga maritima at 2.30 a resolution

Analyse Crystal structure of 2-dehydro-3-deoxyphosphogluconate ALDOLASE/4… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1VLW
Type
protein
Length
616 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-dehydro-3-deoxyphosphogluconate ALDOLASE/4-hydroxy-2- oxoglutarate aldolase
EC
4.1.2.14, 4.1.3.16
UniProt
Q9WXS1
Pockets
6 · best druggability 0.56

Structure

x-ray diffraction · 3 distinct chains · 48% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A2-dehydro-3-deoxyphosphogluconate ALDOLASE/4-hydroxy-2- oxoglutarate aldolase (EC 4.1.2.14, 4.1.3.16)protein20547% helix, 16% strandQ9WXS1
B2-dehydro-3-deoxyphosphogluconate ALDOLASE/4-hydroxy-2- oxoglutarate aldolase (EC 4.1.2.14, 4.1.3.16)protein20748% helix, 17% strandQ9WXS1
C2-dehydro-3-deoxyphosphogluconate ALDOLASE/4-hydroxy-2- oxoglutarate aldolase (EC 4.1.2.14, 4.1.3.16)protein20448% helix, 17% strandQ9WXS1

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13630.560.7550empty
21570.490.7823empty
3870.400.7815empty
4900.360.7523empty
5510.320.7714empty

Interfaces

2 interfaces between chains.

  • B–C · 633 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 230 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 1VLW · Crystal structure of 2-dehydro-3-deoxyphosphogluconate aldolase/4-hydroxy-2-oxoglutarate… · the same entry in another collection · chain A against A, TM-score 1.00

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