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- Publisher Website: 10.4161/cc.5.8.2635
- Scopus: eid_2-s2.0-33746596242
- PMID: 16582588
- WOS: WOS:000238575100001
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Article: CARD tricks: Controlling the interactions of CARD6 with RICK and microtubules
Title | CARD tricks: Controlling the interactions of CARD6 with RICK and microtubules |
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Authors | |
Keywords | ARC Caspase recruitment domain URG4 Aggresome IFN-inducible GTPases Signal transduction Immunity VLIG-1 RICK |
Issue Date | 2006 |
Citation | Cell Cycle, 2006, v. 5, n. 8, p. 797-800 How to Cite? |
Abstract | In recent years, a number of proteins have been identified that contain a homotypic interaction motif called the caspase recruitment domain (CARD). Most proteins containing a CARD are involved in pathways regulating apoptosis or adaptive or innate immunity. Examples of prominent CARD proteins are caspase-9 and Apaf1, which are involved in the intrinsic death pathway; BCL10 and CARD11, which mediate antigen receptor-induced NF-κB activation; and receptor-interacting protein (RIP)-like interacting caspase-like apoptosis regulatory protein kinase (RICK) and the nucleotide-binding oligomerization domain (NOD) proteins, which induce NF-κB activation in response to intracellular bacterial peptidoglycan. The most recently discovered pathway involving CARD proteins senses virally-derived double-stranded (ds) RNA and initiates a host defense signaling program. CARD6 is a CARD-containing protein with a domain structure not shared by any other CARD protein. Although the CARD6 cDNA was deposited in GenBank five years ago, the physiological function of full-length CARD6 has yet to be reported. Here we review our initial characterization of CARD6 and discuss the functional implications of various conserved modules found in the CARD6 protein sequence. We conclude that CARD6 is structurally and potentially functionally related to the superfamily of interferon (IFN)-inducible GTPases, a growing family of host defense proteins that confer cell-autonomous immunity. ©2006 Landes Bioscience. |
Persistent Identifier | http://hdl.handle.net/10722/292578 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 0.947 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Dufner, Almut | - |
dc.contributor.author | Mak, Tak W. | - |
dc.date.accessioned | 2020-11-17T14:56:46Z | - |
dc.date.available | 2020-11-17T14:56:46Z | - |
dc.date.issued | 2006 | - |
dc.identifier.citation | Cell Cycle, 2006, v. 5, n. 8, p. 797-800 | - |
dc.identifier.issn | 1538-4101 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292578 | - |
dc.description.abstract | In recent years, a number of proteins have been identified that contain a homotypic interaction motif called the caspase recruitment domain (CARD). Most proteins containing a CARD are involved in pathways regulating apoptosis or adaptive or innate immunity. Examples of prominent CARD proteins are caspase-9 and Apaf1, which are involved in the intrinsic death pathway; BCL10 and CARD11, which mediate antigen receptor-induced NF-κB activation; and receptor-interacting protein (RIP)-like interacting caspase-like apoptosis regulatory protein kinase (RICK) and the nucleotide-binding oligomerization domain (NOD) proteins, which induce NF-κB activation in response to intracellular bacterial peptidoglycan. The most recently discovered pathway involving CARD proteins senses virally-derived double-stranded (ds) RNA and initiates a host defense signaling program. CARD6 is a CARD-containing protein with a domain structure not shared by any other CARD protein. Although the CARD6 cDNA was deposited in GenBank five years ago, the physiological function of full-length CARD6 has yet to be reported. Here we review our initial characterization of CARD6 and discuss the functional implications of various conserved modules found in the CARD6 protein sequence. We conclude that CARD6 is structurally and potentially functionally related to the superfamily of interferon (IFN)-inducible GTPases, a growing family of host defense proteins that confer cell-autonomous immunity. ©2006 Landes Bioscience. | - |
dc.language | eng | - |
dc.relation.ispartof | Cell Cycle | - |
dc.subject | ARC | - |
dc.subject | Caspase recruitment domain | - |
dc.subject | URG4 | - |
dc.subject | Aggresome | - |
dc.subject | IFN-inducible GTPases | - |
dc.subject | Signal transduction | - |
dc.subject | Immunity | - |
dc.subject | VLIG-1 | - |
dc.subject | RICK | - |
dc.title | CARD tricks: Controlling the interactions of CARD6 with RICK and microtubules | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.4161/cc.5.8.2635 | - |
dc.identifier.pmid | 16582588 | - |
dc.identifier.scopus | eid_2-s2.0-33746596242 | - |
dc.identifier.volume | 5 | - |
dc.identifier.issue | 8 | - |
dc.identifier.spage | 797 | - |
dc.identifier.epage | 800 | - |
dc.identifier.eissn | 1551-4005 | - |
dc.identifier.isi | WOS:000238575100001 | - |
dc.identifier.issnl | 1551-4005 | - |