You are viewing an incomplete version of our website. Please click to reload the website as full version.

Coenzyme Q2 Homolog, Prenyltransferase (Yeast) Proteins (COQ2)

COQ2 encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. Additionally we are shipping COQ2 Antibodies (7) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
COQ2 27235 Q96H96
Rat COQ2 COQ2 498332 Q499N4
COQ2 71883  
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top COQ2 Proteins at antibodies-online.com

Showing 3 out of 4 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 49 to 54 Days
$6,041.49
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 49 to 54 Days
$4,244.78
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details

COQ2 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) Interaction Partners

Fruit Fly (Drosophila melanogaster) Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

  1. flies defective in CoQ biosynthetic gene coq2 were more susceptible to bacterial and fungal infections, while were more resistant to viruses

  2. sbo is an essential gene for Drosophila development, mutation of which leads to an extension of lifespan most likely by altering endogenous CoQ biosynthesis.

Human Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

  1. The V393A variant in the COQ2 gene increases risk of PD.

  2. Results indicated that COQ2 tended to play a population-specific and subtype-depended role in conferring susceptibility to multiple system atrophy

  3. This case-control study shows no evidence for an association between ALS and the V393A variant of COQ2 in Han Chinese.

  4. This study demonstrated that COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.

  5. Multiple system atrophy due to recessive COQ2 mutations (including exon dosage) was not observed in our study

  6. The recessive COQ2 mutations recently were nominated to be the genetic cause in a subset of familial and sporadic MSA (show TPO Proteins) cases.

  7. A novel homozygous mutation in COQ2 (c.905C>T,p.Ala302Val) found in dizygotic twins is linked to fatal infantile multisystem disease.

  8. Functionally impaired variants of COQ2 were associated with an increased risk of multiple-system atrophy in multiplex families and patients with sporadic disease.

  9. Treatment with CoQs having shorter isoprenoid chains, especially CoQ2, induced apoptosis in p53 (show TP53 Proteins)-point mutated BALL-1 cells, whereas treatment with longer isoprenoid chains did not.

  10. Substitution of a highly conserved tyrosine to cysteine at amino acid 297 of COQ2 is the first molecular cause of primary CoQ(10) deficiency.

Mouse (Murine) Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

COQ2 Protein Profile

Protein Summary

This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement.

Gene names and symbols associated with COQ2

  • Coenzyme Q biosynthesis protein 2 (Coq2)
  • coenzyme Q2 4-hydroxybenzoate polyprenyltransferase (COQ2)
  • coenzyme Q2 4-hydroxybenzoate polyprenyltransferase (Coq2)
  • coenzyme Q2 homolog, prenyltransferase (yeast) (coq2)
  • coenzyme Q2 homolog, prenyltransferase (yeast) (COQ2)
  • coenzyme Q2 homolog, prenyltransferase (yeast) (Coq2)
  • Protein COQ-2 (coq-2)
  • 2310002F18Rik protein
  • CG9613 protein
  • CL640 protein
  • coq2 protein
  • COQ10D1 protein
  • Dmel\\CG9613 protein
  • MSA1 protein
  • RGD1306722 protein
  • sbo protein
  • zgc:162600 protein

Protein level used designations for COQ2

CG9613-PA , Coq2-PA , coenzyme Q biosynthesis protein 2 , small boy , 4-hydroxybenzoate polyprenyltransferase, mitochondrial , PHB:polyprenyltransferase , coenzyme Q2 homolog, prenyltransferase , para-hydroxybenzoate-polyprenyltransferase, mitochondrial , para-hydroxybenzoate--polyprenyltransferase, mitochondrial

GENE ID SPECIES
40988 Drosophila melanogaster
27235 Homo sapiens
498332 Rattus norvegicus
100037331 Danio rerio
478457 Canis lupus familiaris
71883 Mus musculus
504633 Bos taurus
175969 Caenorhabditis elegans
Selected quality suppliers for COQ2 Proteins (COQ2)
Did you look for something else?