ATPase Family Gene 3 Like Protein 2 (AFG3L2)

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SCA28; Spinocerebellar Ataxia 28; Paraplegin-like protein

ATPase Family Gene 3 Like Protein 2 (AFG3L2)
AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly. AFG3L2 encodes a deduced 797-amino acid protein whose sequence shows 69% similarity to the yeast Afg3 mitochondrial ATPase and 49% identity to paraplegin. AFG3L2 contains an AAA (for ATPase associated with diverse cellular activities) domain of about 190 amino acids with an ATP/GTP-binding site, a zinc-dependent binding domain, and an RNA-binding region. Northern blot analysis revealed that AFG3L2 is expressed ubiquitously as a 3.2-kb transcript in fetal and adult tissues, with greatest expression in heart and skeletal muscle.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant ATPase Family Gene 3 Like Protein 2 (AFG3L2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) CLIA Kit Customized Service Offer
n/a ELISA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant ATPase Family Gene 3 Like Protein 2 (AFG3L2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) CLIA Kit Customized Service Offer
n/a ELISA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant ATPase Family Gene 3 Like Protein 2 (AFG3L2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to ATPase Family Gene 3 Like Protein 2 (AFG3L2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) CLIA Kit Customized Service Offer
n/a ELISA Kit for ATPase Family Gene 3 Like Protein 2 (AFG3L2) ELISA Kit Customized Service Offer
  1. "Identification and characterization of AFG3L2, a novel paraplegin-related gene."Genomics 59:51-58(1999) [PubMed] [Europe PMC] [Abstract]
  2. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  3. "Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia."J. Cell Biol. 163:777-787(2003) [PubMed] [Europe PMC] [Abstract]
  4. "Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia."Mol. Cell. Biol. 27:758-767(2007) [PubMed] [Europe PMC] [Abstract]
  5. "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
  6. "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
  7. "Northeast structural genomics consortium target HR6741A."Submitted (MAR-2012) to the PDB data bank
  8. "Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation."Eur. J. Hum. Genet. 18:965-968(2010) [PubMed] [Europe PMC] [Abstract]
  9. "Missense mutations in the AFG3L2 proteolytic domain account for approximately 1.5% of European autosomal dominant cerebellar ataxias."Hum. Mutat. 31:1117-1124(2010) [PubMed] [Europe PMC] [Abstract]
  10. "Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28." Nat. Genet. 42:313-321(2010) [PubMed] [Europe PMC] [Abstract]
  11. "Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases." PLoS Genet. 7:E1002325-E1002325(2011) [PubMed] [Europe PMC] [Abstract]