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Programmed cell death 11

NF-kappaB-binding protein, NFBP, ALG-4
PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation of 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008] (from NCBI)
Top mentioned proteins: NF-kappaB, p65, Rel, AP-1, CAN
Papers on NF-kappaB-binding protein
Differential impact of the HEN1 homolog HENN-1 on 21U and 26G RNAs in the germline of Caenorhabditis elegans.
Ketting et al., Utrecht, Netherlands. In Plos Genet, 2011
Within the 26G RNA class, we find that specifically ERGO-1-bound 26G RNAs are modified by HENN-1, while ALG-3/ALG-4-bound 26G RNAs are not.
Argonautes ALG-3 and ALG-4 are required for spermatogenesis-specific 26G-RNAs and thermotolerant sperm in Caenorhabditis elegans.
Mello et al., Worcester, United States. In Proc Natl Acad Sci U S A, 2010
Here we describe the role of two AGO-class paralogs, alg-3 (T22B3.2) and alg-4 (ZK757.3), in promoting thermotolerant male fertility.
A novel small-subunit processome assembly intermediate that contains the U3 snoRNP, nucleolin, RRP5, and DBP4.
Watkins et al., Newcastle upon Tyne, United Kingdom. In Mol Cell Biol, 2009
The 50S U3 snoRNP is an small subunit assembly intermediate that is likely recruited to the pre-rRNA through the RNA-binding proteins nucleolin and RRP5.[RRP5, DBP4]
Evidence for involvement of NFBP in processing of ribosomal RNA.
Amini et al., Philadelphia, United States. In J Cell Physiol, 2008
Evidence is presented for involvement of PDCD11 in processing of ribosomal RNA.
[Effect of hemoperfusion treated plasma from patients with chronic severe hepatitis on the activity and expression of CYP4503A in C3A cells].
Duan et al., Beijing, China. In Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 2007
There were four groups in the experiment: normal fetal bovine plasma (NFBP) group, normal human plasma (NHP) group, hemoperfusion plasma (HPP) group, chronic severe hepatitis plasma (CSHP) group.
Transcriptional regulation of the human GD3 synthase gene expression in Fas-induced Jurkat T cells: a critical role of transcription factor NF-kappaB in regulated expression.
Kim et al., Taej┼Ćn, South Korea. In Glycobiology, 2006
In addition, the translocation of NF-kappaB-binding protein to nucleus by Fas activation is also crucial for the increased expression of the GD3 synthase gene in Fas-activated Jurkat T cells.
Interplay between NFBP and NF-kappaB modulates tat activation of the LTR.
Amini et al., Philadelphia, United States. In J Cell Physiol, 2005
Here, we report on the physical and functional interaction of NFBP, a recently identified protein that interacts with the P65 subunit of NF-kappaB, with HIV-1 Tat.
Identification of a novel protein from glial cells based on its ability to interact with NF-kappaB subunits.
Amini et al., Philadelphia, United States. In J Cell Biochem, 2004
This gene, named NF-kappaB-binding protein (NFBP) is located on chromosome 10q24.2-25.1 and hybridized to a single transcript of nearly 6 kb in size.
Function and regulation of the CD95 (APO-1/Fas) ligand in the immune system.
Krammer et al., Heidelberg, Germany. In Semin Immunol, 2003
In this review, we present a survey of the role of the CD95/CD95L system in the immune system and, particularly, focus on the signals and transcription factors (NF-AT, Egr, NF-kappaB, AP-1, c-Myc, Nur77, IRFs, SP-1, ALG-4, ROR(gamma)t, and CIITA) involved in CD95L expression.
Nuclear factor-kappaB p50 is required for tumor necrosis factor-alpha-induced colony-stimulating factor-1 gene expression in osteoblasts.
Weir et al., New Haven, United States. In Endocrinology, 2000
As determined by electrophoretic mobility shift assays, antiserum against the NF-kappaB-binding protein, p50, retarded the mobility of the inducible complex, whereas antisera against p52, p65, c-Rel, Rel B, IkappaB alpha, IkappaB gamma, and Bcl-3 had no effect.
Identification of NF-kappaB in the marine fish Stenotomus chrysops and examination of its activation by aryl hydrocarbon receptor agonists.
Stegeman et al., United States. In Chem Biol Interact, 2000
In addition, an approximately 35kD NF-kappaB binding protein was evident in liver and kidney.
Constitutive activation of transcription factors NF-(kappa)B, AP-1, and NF-IL6 in human head and neck squamous cell carcinoma cell lines that express pro-inflammatory and pro-angiogenic cytokines.
Van Waes et al., Bethesda, United States. In Mol Carcinog, 1999
Supershift analysis with antibodies specific for NF-kappaB, AP-1, and NF-IL6 binding proteins showed that the NF-kappaB-binding protein included p65/Rel A and p50; AP-1 activity included c-jun, junB, junD, and Fra-1; and NF-IL6 included C/EBPbeta.
Regulation of Fas ligand expression and cell death by apoptosis-linked gene 4.
D'Adamio et al., Bethesda, United States. In Nat Med, 1999
Overexpression of full-length ALG-4 induced transcription of FasL and, consequently, apoptosis.
Regulation of NF-kappa B activity in rat dorsal root ganglia and PC12 cells by tumour necrosis factor and nerve growth factor.
Wood, London, United Kingdom. In Neurosci Lett, 1995
South-western blots show the presence of a single NF-kappa B binding protein with picomolar affinity, co-migrating with NF-kappa B2 (p49/p52) immunoreactive material in dorsal root ganglia.
Regulatory elements involved in tax-mediated transactivation of the HTLV-I LTR.
Gaynor et al., Dallas, United States. In Virology, 1993
We demonstrated that an NF-kappa B binding protein, PRDII-BF1, but not the rel protein, bound to the B and C motifs in the 21-bp repeat.
Identification of NF-jun, a novel inducible transcription factor that regulates c-jun gene transcription.
Kufe et al., Boston, United States. In Embo J, 1992
Our findings also indicate that while NF-jun has several features in common with the NF-kappa B binding protein including its subcellular localization and its ability to translocate from the cytoplasm to the nucleus, this factor recognizes a unique DNA sequence.
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