Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13)

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Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13)
Kelch is a 50-residue motif, named after the Drosophila mutant in which it was first identified. This sequence motif represents one beta-sheet blade, and several of these repeats can associate to form a beta-propeller. For instance, the motif appears 6 times in Drosophila egg-chamber regulatory protein, creating a 6-bladed beta-propeller. The motif is also found in mouse protein MIPP and in a number of poxviruses.
Defects in KBTBD13 are the cause of nemaline myopathy type 6 (NEM6). A form of nemaline myopathy characterized by childhood onset of slowly progressive proximal muscle weakness, exercise intolerance, and slow movements with stiff muscles. Patients are unable to run or correct themselves from falling over.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13) CLIA Kit Customized Service Offer
n/a ELISA Kit for Kelch Repeat And BTB Domain Containing Protein 13 (KBTBD13) ELISA Kit Customized Service Offer
  1. "Analysis of the DNA sequence and duplication history of human chromosome 15." Nature 440:671-675(2006) [PubMed] [Europe PMC] [Abstract]
  2. "KBTBD13 interacts with Cullin 3 to form a functional ubiquitin ligase."Biochem. Biophys. Res. Commun. 421:743-749(2012) [PubMed] [Europe PMC] [Abstract]
  3. "Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores." Am. J. Hum. Genet. 87:842-847(2010) [PubMed] [Europe PMC] [Abstract]