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Transcription elongation factor B

110-kDa, NIP1, eIF3c, BNIP1
This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. In addition, this protein is involved in vesicle transport into the endoplasmic reticulum. Alternative splicing of this gene results in four protein products with identical N- and C-termini. [provided by RefSeq, Mar 2011] (from NCBI)
Top mentioned proteins: ACID, CAN, HAD, fibrillin-1, CD45
Papers on 110-kDa
Biological insights into the expression of translation initiation factors from recombinant CHOK1SV cell lines and their relationship to enhanced productivity.
Smales et al., Andover, United States. In Biochem J, Jan 2016
We have determined mRNA and protein levels of the key components of the closed loop, eIFs (eIF3a, eIF3b, eIF3c, eIF3h, eIF3i and eIF4G1), poly(A)-binding protein (PABP) 1 and PABP-interacting protein 1 (PAIP1), across a panel of 30 recombinant mAb-producing GS-CHOK1SV cell lines with a broad range of growth characteristics and production levels of a model recombinant mAb.
Affinity maturation of anti-(4-hydroxy-3-nitrophenyl)acetyl antibodies accompanies a modulation of antigen specificity.
Azuma et al., Kyoto, Japan. In Mol Immunol, Jan 2016
We address here the question of whether affinity maturation accompanies in the fine specificity of these antibodies by analyzing the interaction between NP1-, NIP1-, or NNP1-hen egg lysozyme and anti-NP antibodies that possess different association constants to NP using a surface plasmon resonance biosensor.
Genomewide Histone H3 Lysine 9 Acetylation Profiling in CD4+ T Cells Revealed Endoplasmic Reticulum Stress Deficiency in Patients with Acute-on-chronic Liver Failure.
He et al., Xi'an, China. In Scand J Immunol, Nov 2015
Functional analysis showed endoplasmic reticulum (ER) stress, or downstream pathway-related genes, such as BIP, ATF4, PER1, CSNK1D, IRF3, BNIP1, AKT1 and UBC, were differentially modified in ACLF.
Identification of target antigens of naturally occurring autoantibodies in cerebrospinal fluid.
Inuzuka et al., Gifu, Japan. In J Proteomics, Nov 2015
These antigen spots were identified as heat shock 105-kDa/110-kDa protein 1, isoform CRA_b, 78-kDa glucose-regulated protein, heat shock cognate 71-kDa protein, tubulin beta chain, vimentin (2 spots), and 60-kDa heat shock protein, mitochondrial; we could not identify the protein name corresponding to 1 of the 8 spots.
Assessment and modelling of Ni(II) retention by an ion-imprinted polymer: application in natural samples.
Branger et al., La Garde, France. In J Colloid Interface Sci, Jul 2015
Non-Imprinted Polymers (NIP1, NIP2 and NIP3) were prepared as control polymers in similar conditions but with pure VbIDA instead of VbIDA-Ni.
Eukaryotic initiation factor 3C silencing inhibits cell proliferation and promotes apoptosis in human glioma.
Jiao et al., China. In Oncol Rep, Jun 2015
Eukaryotic initiation factor 3, subunit c (eIF3c), an oncogene overexpressed in human cancers, plays an important role in cell tumorigenesis and proliferation.
Eukaryotic translation initiation factor 3, subunit C is overexpressed and promotes cell proliferation in human glioma U-87 MG cells.
Jiao et al., Shijiazhuang, China. In Oncol Lett, Jun 2015
The present study explored the expression and the role of eIF 3, subunit C (eIF3c) in human glioma.
TANGO1 recruits ERGIC membranes to the endoplasmic reticulum for procollagen export.
Malhotra et al., Barcelona, Spain. In Elife, 2014
Along with the t-SNARE Syntaxin 18, we now reveal the complete complement of SNAREs required in this process, t-SNAREs BNIP1 and USE1, and v-SNARE YKT6.
Functional characterization of the role of the N-terminal domain of the c/Nip1 subunit of eukaryotic initiation factor 3 (eIF3) in AUG recognition.
Valášek et al., Praha, Czech Republic. In J Biol Chem, 2012
binding of eIF1 to the c/Nip1-NTD is equally important for its initial recruitment to PICs and for its proper functioning in selecting the translational start site
Endoplasmic reticulum-specific BH3-only protein BNIP1 induces mitochondrial fragmentation in a Bcl-2- and Drp1-dependent manner.
Choi et al., Taejŏn, South Korea. In J Cell Physiol, 2012
ER-specific BNIP1 plays an important role in mitochondrial dynamics by modulating the mitochondrial fission protein Drp1
Differential expression of BNIP family members of BH3-only proteins during the development and after axotomy in the rat.
Geum et al., Seoul, South Korea. In Mol Cells, 2012
three members of the BNIP family, BNIP1, BNIP3 and BNIP3L, are expressed in the developing brain with distinct brain region specificity
The interaction between human initiation factor eIF3 subunit c and heat-shock protein 90: a necessary factor for translation mediated by the hepatitis C virus internal ribosome entry site.
Takaku et al., Narashino, Japan. In Virus Res, 2012
These results indicate that the interaction between Hsp90 and eIF3c may play an important role in hepatitis C virus internal ribosome entry site-mediated translation.
RNF185, a novel mitochondrial ubiquitin E3 ligase, regulates autophagy through interaction with BNIP1.
Tang et al., Beijing, China. In Plos One, 2010
Human BNIP1 colocalizes with RNF185 at mitochondria and is polyubiquitinated by RNF185 through K63-based ubiquitin linkage in vivo.
Dipeptidyl peptidase in autoimmune pathophysiology.
Morimoto et al., Tokyo, Japan. In Adv Clin Chem, 2010
CD26 is a 110-kDa surface glycoprotein with intrinsic dipeptidyl peptidase IV (DPPIV) activity that is expressed on various cell types and has many biological functions.
The regulation of class IA PI 3-kinases by inter-subunit interactions.
Backer, United States. In Curr Top Microbiol Immunol, 2009
The class IA PI 3-kinase is a heterodimer consisting of one regulatory subunit (p85α, p85β, p55α, p50α, or p55γ) and one 110-kDa catalytic subunit (p110α, β or δ).
The mRNA export factor Gle1 and inositol hexakisphosphate regulate distinct stages of translation.
Wente et al., Nashville, United States. In Cell, 2008
In addition, Gle1 has a conserved physical association with the initiation factor eIF3, and gle1 mutants display genetic interactions with the eIF3 mutant nip1-1.
The merlin interacting proteins reveal multiple targets for NF2 therapy.
Scoles, Los Angeles, United States. In Biochim Biophys Acta, 2008
In efforts to determine merlin function several groups have discovered 34 merlin interacting proteins, including ezrin, radixin, moesin, CD44, layilin, paxillin, actin, N-WASP, betaII-spectrin, microtubules, TRBP, eIF3c, PIKE, NHERF, MAP, RalGDS, RhoGDI, EG1/magicin, HEI10, HRS, syntenin, caspr/paranodin, DCC, NGB, CRM1/exportin, SCHIP1, MYPT-1-PP1delta, RIbeta, PKA, PAK (three types), calpain and Drosophila expanded.
Matrix-degrading podosomes in smooth muscle cells.
Gimona et al., Salzburg, Austria. In Eur J Cell Biol, 2006
The molecular basis for this local inhibition of contractility includes the clustering of cortactin during podosome formation (which precedes the rapid, local dispersion of myosin, tropomyosin and h1 calponin), and the specific recruitment of 110-kDa actin filament-associated protein (AFAP-110) and 190-kDa Rho-specific GTPase-activating protein (p190RhoGAP) to the microdomains.
Structure of the cyclic-AMP-responsive exchange factor Epac2 in its auto-inhibited state.
Bos et al., Utrecht, Netherlands. In Nature, 2006
Here we report the three-dimensional structure of full-length Epac2, a 110-kDa protein that contains an amino-terminal regulatory region with two cyclic-nucleotide-binding domains and a carboxy-terminal catalytic region.
Dipeptidyl peptidase IV in tumor progression.
Mizutani et al., Nagoya, Japan. In Biochim Biophys Acta, 2005
Dipeptidyl peptidase IV (DPPIV) is a 110-kDa glycoprotein with ubiquitous expression.
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