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Crystal structure of dihydroorotate dehydrogenase from leishmania major in complex with phenyl isothiocyanate

Analyse Crystal structure of dihydroorotate dehydrogenase from leishmania major in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4EF8
Type
protein
Length
627 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydroorotate dehydrogenase
EC
1.3.3.1
UniProt
Q4QEW7
Ligands
FMN, 0FI, SO4
Pockets
5 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydroorotate dehydrogenase (EC 1.3.3.1)protein31340% helix, 23% strandQ4QEW7
BDihydroorotate dehydrogenase (EC 1.3.3.1)protein31439% helix, 23% strandQ4QEW7

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B
  • 0FI · N-phenylthioformamide · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15940.790.8562FMN
25520.790.8564FMN
31300.560.8220GOL
41310.470.7720GOL
51340.440.7619GOL

Interfaces

1 interface between chains.

  • A–B · 2394 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 4EF8 · Crystal structure of dihydroorotate dehydrogenase from Leishmania major in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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