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Crystal structure of aconitase with trans-aconitate and nitrocitrate bound

Analyse Crystal structure of aconitase with trans-aconitate and nitrocitrate bound in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1NIT
Type
protein
Length
753 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aconitase
EC
4.2.1.3
UniProt
P20004
Ligands
SF4, SO4
Pockets
9 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAconitase (EC 4.2.1.3)protein75335% helix, 21% strandP20004

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · chains A
  • SO4 · Sulfate ion · ion · chains A

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

Pockets

9 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1790.750.9827SO4, SF4
2750.730.9724empty
33110.620.7948empty
42520.540.7739empty
51470.500.7927empty

Compared structures

  • 1NIT · Crystal structure of aconitase with trans-aconitate and nitrocitrate bound · the same entry in another collection · chain A against A, TM-score 1.00
  • P20004 · AlphaFold monomer V2.0 prediction for aconitate hydratase, mitochondrial (P20004) · a predicted model of the same protein · chain A against A, TM-score 1.00

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