| Literature DB >> 11374873 |
B J Geddes1, L Wang, W J Huang, M Lavellee, G A Manji, M Brown, M Jurman, J Cao, J Morgenstern, S Merriam, M A Glucksmann, P S DiStefano, J Bertin.
Abstract
The CED4/Apaf-1 family of proteins functions as critical regulators of apoptosis and NF-kappaB signaling pathways. A novel human member of this family, called CARD12, was identified that induces apoptosis when expressed in cells. CARD12 is most similar in structure to the CED4/Apaf-1 family member CARD4, and is comprised of an N-terminal caspase recruitment domain (CARD), a central nucleotide-binding site (NBS), and a C-terminal domain of leucine-rich repeats (LRR). The CARD domain of CARD12 interacts selectively with the CARD domain of ASC, a recently identified proapoptotic protein. In addition, CARD12 coprecipitates caspase-1, a caspase that participates in both apoptotic signaling and cytokine processing. CARD12 may assemble with proapoptotic CARD proteins to coordinate the activation of downstream apoptotic and inflammatory signaling pathways. Copyright 2001 Academic Press.Entities:
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Year: 2001 PMID: 11374873 DOI: 10.1006/bbrc.2001.4928
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575