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Crystal Structure of Mycobacterium tuberculosis Shikimate Dehydrogenase

Analyse Crystal Structure of Mycobacterium tuberculosis Shikimate Dehydrogenase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4P4G
Type
protein
Length
525 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.7
Source
Mycobacterium tuberculosis
Molecule
Shikimate 5-dehydrogenase AroE (5-dehydroshikimate reductase)
EC
1.1.1.25
UniProt
P95001
Ligands
SKM, BR, SO4
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · resolution 1.7 · 2 distinct chains · 45% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AShikimate 5-dehydrogenase AroE (5-dehydroshikimate reductase) (EC 1.1.1.25)protein26544% helix, 22% strandP95001
BShikimate 5-dehydrogenase AroE (5-dehydroshikimate reductase) (EC 1.1.1.25)protein26045% helix, 21% strandP95001

Ligands and binding sites

  • SKM · (3R,4S,5R)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid · ligand · chains A
  • BR · Bromide ion · ion · 7 copies · chains A, B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15580.760.8371SKM, BR, SO4
22750.680.8429BR
3750.390.7819empty
4670.350.7716SO4
5730.340.7619empty

Interfaces

1 interface between chains.

  • A–B · 620 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 4P4G · Crystal structure of mycobacterium tuberculosis shikimate dehydrogenase · the same entry in another collection · chain A against A, TM-score 1.00

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