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Crystal structure of acireductone dioxygenase (13543033) from mus musculus at 2.06 a resolution

Analyse Crystal structure of acireductone dioxygenase (13543033) from mus musculus at… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1VR3
Type
protein
Length
179 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acireductone dioxygenase
EC
1.13.11.-
UniProt
Q99JT9
Ligands
UNL, NI
Pockets
1 · best druggability 0.63

Structure

x-ray diffraction · 1 distinct chain · 22% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcireductone dioxygenase (EC 1.13.11.-)protein17922% helix, 34% strandQ99JT9

Ligands and binding sites

  • UNL · Unknown ligand · ligand · chains A
  • NI · Nickel (II) ion · metal · chains A
  • IPA · Isopropyl alcohol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11460.630.8522UNL

Modifications

Observed in the structure: 9 modified (engineered).

Compared structures

  • 1VR3 · Crystal structure of Acireductone dioxygenase (13543033) from Mus musculus at 2.06 A… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q99JT9 · AlphaFold monomer V2.0 prediction for 1,2-dihydroxy-3-keto-5-methylthiopentene… · a predicted model of the same protein · chain A against A, TM-score 0.98

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