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Crystal structure of yeast COQ5 in the apo form

Analyse Crystal structure of yeast COQ5 in the apo form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OBX
Type
protein
Length
940 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
EC
2.1.1.201
UniProt
P49017
Ligands
TAM
Pockets
10 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, C, B2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial (EC 2.1.1.201)protein23549% helix, 22% strandP49017

Ligands and binding sites

  • TAM · Tris(hydroxyethyl)aminomethane · ligand · 2 copies · chains A, D, C, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111110.740.7789empty
26290.690.7775empty
32550.660.8339empty
42390.660.8336empty
5680.480.8320empty

Interfaces

6 interfaces between chains.

  • A–B · 1057 Ų buried · 0 hydrogen bonds · protein-protein
  • D–C · 1051 Ų buried · 0 hydrogen bonds · protein-protein
  • A–D · 261 Ų buried · 3 hydrogen bonds · protein-protein
  • C–B · 258 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 41 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4OBX · Crystal structure of yeast Coq5 in the apo form · the same entry in another collection · chain B against B, TM-score 1.00
  • P49017 · AlphaFold monomer V2.0 prediction for 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase… · a predicted model of the same protein · chain D against A, TM-score 0.98

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