Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2004-8-25
pubmed:abstractText
The activation of NF-kappaB and IKK requires an upstream kinase complex consisting of TAK1 and adaptor proteins such as TAB1, TAB2, or TAB3. TAK1 is in turn activated by TRAF6, a RING domain ubiquitin ligase that facilitates the synthesis of lysine 63-linked polyubiquitin chains. Here we present evidence that TAB2 and TAB3 are receptors that bind preferentially to lysine 63-linked polyubiquitin chains through a highly conserved zinc finger (ZnF) domain. Mutations of the ZnF domain abolish the ability of TAB2 and TAB3 to bind polyubiquitin chains, as well as their ability to activate TAK1 and IKK. Significantly, replacement of the ZnF domain with a heterologous ubiquitin binding domain restored the ability of TAB2 and TAB3 to activate TAK1 and IKK. We also show that TAB2 binds to polyubiquitinated RIP following TNFalpha stimulation. These results indicate that polyubiquitin binding domains represent a new class of signaling domains that regulate protein kinase activity through a nonproteolytic mechanism.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing, http://linkedlifedata.com/resource/pubmed/chemical/CHUK protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/I-kappa B Kinase, http://linkedlifedata.com/resource/pubmed/chemical/IKBKB protein, human, http://linkedlifedata.com/resource/pubmed/chemical/IKBKE protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/MAP Kinase Kinase Kinases, http://linkedlifedata.com/resource/pubmed/chemical/MAP kinase kinase kinase 7, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B, http://linkedlifedata.com/resource/pubmed/chemical/Polyubiquitin, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RIPK1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Receptor-Interacting Protein..., http://linkedlifedata.com/resource/pubmed/chemical/TAB2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TAB3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TNF Receptor-Associated Factor 6, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1097-2765
pubmed:author
pubmed:issnType
Print
pubmed:day
27
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
535-48
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:15327770-Adaptor Proteins, Signal Transducing, pubmed-meshheading:15327770-Amino Acid Sequence, pubmed-meshheading:15327770-Carrier Proteins, pubmed-meshheading:15327770-Cell Line, pubmed-meshheading:15327770-Enzyme Activation, pubmed-meshheading:15327770-Humans, pubmed-meshheading:15327770-I-kappa B Kinase, pubmed-meshheading:15327770-Interleukin-1, pubmed-meshheading:15327770-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:15327770-MAP Kinase Kinase Kinases, pubmed-meshheading:15327770-Models, Biological, pubmed-meshheading:15327770-Molecular Sequence Data, pubmed-meshheading:15327770-NF-kappa B, pubmed-meshheading:15327770-Polyubiquitin, pubmed-meshheading:15327770-Protein Binding, pubmed-meshheading:15327770-Protein-Serine-Threonine Kinases, pubmed-meshheading:15327770-Proteins, pubmed-meshheading:15327770-Receptor-Interacting Protein Serine-Threonine Kinases, pubmed-meshheading:15327770-Sequence Alignment, pubmed-meshheading:15327770-Signal Transduction, pubmed-meshheading:15327770-TNF Receptor-Associated Factor 6, pubmed-meshheading:15327770-Tumor Necrosis Factor-alpha, pubmed-meshheading:15327770-Zinc Fingers
pubmed:year
2004
pubmed:articleTitle
TAB2 and TAB3 activate the NF-kappaB pathway through binding to polyubiquitin chains.
pubmed:affiliation
Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't