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Crystal structure of human dihydroorotate dehydrogenase (dhodh) with 057

Analyse Crystal structure of human dihydroorotate dehydrogenase (dhodh) with 057 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JS3
Type
protein
Length
365 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydroorotate dehydrogenase (quinone), mitochondrial
EC
1.3.5.2
UniProt
Q02127
Ligands
FMN, ORO, JS3, SO4
Pockets
4 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydroorotate dehydrogenase (quinone), mitochondrial (EC 1.3.5.2)protein36547% helix, 16% strandQ02127

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · chains A
  • ORO · Orotic acid · ligand · chains A
  • JS3 · 2-chloro-4-methyl-N-(naphthalen-2-yl)-1,3-thiazole-5-carboxamide · ligand · chains A
  • SO4 · Sulfate ion · ion · 7 copies · chains A
  • ACY · Acetic acid · additive · 5 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13910.840.9262FMN, ORO, JS3, ACY
21170.500.8128empty
3890.450.8020SO4
4860.380.7716ACY

Compared structures

  • 4JS3 · Crystal structure of human dihydroorotate dehydrogenase (DHODH) with 057 · the same entry in another collection · chain A against A, TM-score 1.00

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