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COMMD proteins, a novel family of structural and functional homologs of MURR1.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2005 Jun 10; Vol. 280 (23), pp. 22222-32. Date of Electronic Publication: 2005 Mar 30. - Publication Year :
- 2005
-
Abstract
- MURR1 is a multifunctional protein that inhibits nuclear factor kappaB (NF-kappaB), a transcription factor with pleiotropic functions affecting innate and adaptive immunity, apoptosis, cell cycle regulation, and oncogenesis. Here we report the discovery of a new family of proteins with homology to MURR1. These proteins form multimeric complexes and were identified in a biochemical screen for MURR1-associated factors. The family is defined by the presence of a conserved and unique motif termed the COMM (copper metabolism gene MURR1) domain, which functions as an interface for protein-protein interactions. Like MURR1, several of these factors also associate with and inhibit NF-kappaB. The proteins designated as COMMD or COMM domain containing 1-10 are extensively conserved in multicellular eukaryotic organisms and define a novel family of structural and functional homologs of MURR1. The prototype of this family, MURR1/COMMD1, suppresses NF-kappaB not by affecting nuclear translocation or binding of NF-kappaB to cognate motifs; rather, it functions in the nucleus by affecting the association of NF-kappaB with chromatin.
- Subjects :
- Active Transport, Cell Nucleus
Adaptor Proteins, Signal Transducing
Amino Acid Motifs
Amino Acid Sequence
Animals
Apoptosis
Carrier Proteins
Cell Cycle
Cell Line
Cell Nucleus metabolism
Chromatin metabolism
Chromatin Immunoprecipitation
Glutathione Transferase metabolism
Humans
Immunoblotting
Immunoprecipitation
Luciferases metabolism
Microscopy, Confocal
Microscopy, Fluorescence
Molecular Sequence Data
NF-kappa B metabolism
Plasmids metabolism
Protein Binding
Protein Structure, Tertiary
Proteins metabolism
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Amino Acid
Subcellular Fractions metabolism
Transfection
Proteins physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 280
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 15799966
- Full Text :
- https://doi.org/10.1074/jbc.M501928200