BCS1 Like Protein (BCS1L)

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BCS; BCS1; FLNMS; GRACILE; Hs.6719; h-BCS; GRACILE Syndrome; Bjornstad Syndrome; Mitochondrial chaperone BCS1

BCS1 Like Protein (BCS1L)
BCS1L encodes a homolog of the S. cerevisiae bcs1 protein which is involved in the assembly of complex III of the mitochondrial respiratory chain. The encoded protein does not contain a mitochondrial targeting sequence but experimental studies confirm that it is imported into mitochondria. Mutations in this gene are associated with mitochondrial complex III deficiency and the GRACILE syndrome. Two alternatively spliced transcripts encoding the same protein have been described.The predicted 420-amino acid human protein is 50% identical to yeast bcs1 and, like bcs1, contains 2 conserved nucleotide-binding motifs. Although BCS1L does not contain an N-terminal mitochondrial targeting sequence, in vitro mitochondrial import and trypsin-protection assays demonstrated that it is imported into mitochondria.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant BCS1 Like Protein (BCS1L) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to BCS1 Like Protein (BCS1L) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to BCS1 Like Protein (BCS1L) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for BCS1 Like Protein (BCS1L) CLIA Kit Customized Service Offer
n/a ELISA Kit for BCS1 Like Protein (BCS1L) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant BCS1 Like Protein (BCS1L) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to BCS1 Like Protein (BCS1L) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to BCS1 Like Protein (BCS1L) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for BCS1 Like Protein (BCS1L) CLIA Kit Customized Service Offer
n/a ELISA Kit for BCS1 Like Protein (BCS1L) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant BCS1 Like Protein (BCS1L) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to BCS1 Like Protein (BCS1L) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to BCS1 Like Protein (BCS1L) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for BCS1 Like Protein (BCS1L) CLIA Kit Customized Service Offer
n/a ELISA Kit for BCS1 Like Protein (BCS1L) ELISA Kit Customized Service Offer
  1. "Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain."Genomics 54:494-504(1998) [PubMed] [Europe PMC] [Abstract]
  2. "A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure."Nat. Genet. 29:57-60(2001) [PubMed] [Europe PMC] [Abstract]
  3. "GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L."Am. J. Hum. Genet. 71:863-876(2002) [PubMed] [Europe PMC] [Abstract]
  4. "Large-scale concatenation cDNA sequencing."Genome Res. 7:353-358(1997) [PubMed] [Europe PMC] [Abstract]
  5. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  6. "The full-ORF clone resource of the German cDNA consortium."BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
  7. "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]
  8. "Characterization of the mitochondrial protein LETM1, which maintains the mitochondrial tubular shapes and interacts with the AAA-ATPase BCS1L."J. Cell Sci. 121:2588-2600(2008) [PubMed] [Europe PMC] [Abstract]
  9. "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
  10. "Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene."Am. J. Med. Genet. A 121:126-131(2003) [PubMed] [Europe PMC] [Abstract]
  11. "Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy."Hum. Mol. Genet. 16:1241-1252(2007) [PubMed] [Europe PMC] [Abstract]
  12. "Missense mutations in the BCS1L gene as a cause of the Bjoernstad syndrome."N. Engl. J. Med. 356:809-819(2007) [PubMed] [Europe PMC] [Abstract]
  13. "Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient."Neuromuscul. Disord. 19:143-146(2009) [PubMed] [Europe PMC] [Abstract]
  14. "Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome."J. Hum. Genet. 58:819-821(2013) [PubMed] [Europe PMC] [Abstract]
  15. "Clinical and biochemical features associated with BCS1L mutation."J. Inherit. Metab. Dis. 36:813-820(2013) [PubMed] [Europe PMC] [Abstract]