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G3BP1 encodes one of the DNA-unwinding enzymes which prefers partially unwound 3'-tailed substrates and can also unwind partial RNA/DNA and RNA/RNA duplexes in an ATP-dependent fashion. 再加上，我们可以发GTPase Activating Protein (SH3 Domain) Binding Protein 1 抗体 (153) 和 GTPase Activating Protein (SH3 Domain) Binding Protein 1 蛋白 (13)和数多这个蛋白质的别的产品。
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Activated glucocorticoid receptor (显示 NR3C1 ELISA试剂盒) induced phosphorylation of v-AKT (显示 AKT1 ELISA试剂盒) Murine Thymoma Viral Oncogene (显示 RAB1A ELISA试剂盒) Homologue (AKT (显示 AKT1 ELISA试剂盒)) kinase, which in turn phosphorylated and promoted nuclear translocation of G3BP1. The nuclear G3BP1 bound to the G3BP1 consensus sequence located on primary miR (显示 MLXIP ELISA试剂盒)-15b~16-2 and miR (显示 MLXIP ELISA试剂盒)-23a~27a~24-2 to inhibit their maturation.
Results show the crystal structure of the NTF2 (显示 NUTF2 ELISA试剂盒)-like domain of G3BP-1 in complex with nsP3 (显示 SH2D3C ELISA试剂盒) protein revealing a poly-complex of G3BP-1 dimers interconnected through the FGDF motifs in nsP3 (显示 SH2D3C ELISA试剂盒). Although in vitro and in vivo binding studies revealed a hierarchical interaction of the two FGDF motifs with G3BP-1, viral growth curves clearly demonstrated that two intact FGDF motifs are required for efficient viral replication.
Based on insights from the structures and existing biochemical data, the existence of an evolutionarily conserved ribonucleoprotein (显示 RBP31 ELISA试剂盒) (RNP (显示 RNPC3 ELISA试剂盒)) complex consisting of Caprin-1, FMRP (显示 FMR1 ELISA试剂盒) and G3BP1 is proposed.
G3BP1 interacts directly with the foot-and-mouth disease virus internal ribosome entry site and negatively regulates translation.
The data suggested that JNK (显示 MAPK8 ELISA试剂盒)-enhanced Tudor-SN phosphorylation promotes the interaction between Tudor-SN and G3BP and facilitates the efficient recruitment of Tudor-SN into stress granules under conditions of sodium arsenite-induced oxidative stress.
These data support a role for casein kinase 2 in regulation of protein synthesis by downregulating stress granule formation through G3BP1.
G3BP1 is differentially methylated on specific arginine residues by protein arginine methyltransferase (显示 PRMT1 ELISA试剂盒) (PRMT) 1 (显示 PRMT1 ELISA试剂盒) and PRMT5 (显示 PRMT5 ELISA试剂盒) in its RGG domain.
Our data define G3BP1 as a novel independent prognostic factor that is correlated with gastric cancer progression.
G3BP mediates the condensation of stress granules by shifting between two different states that are controlled by the phosphorylation of S149 and by binding to Caprin1 or USP10 (显示 USP10 ELISA试剂盒).
Host G3BP1 captures HIV-1 RNA transcripts and thereby restricts mRNA translation, viral protein production and virus particle formation.
the aberrant mutant SOD1 (显示 SOD1 ELISA试剂盒)-G3BP1 interaction affects stress granule dynamics
G3BP is involved in a new functional mechanism to regulate non-coding RNAs including intron-retaining transcripts, and thus have broad implications for neuronal gene regulation, where intron retention is widespread
G3bp1 posttranscriptionally regulates miRNA-1 processing in the heart.
Our findings identified a novel function of G3BP1 in the progression of breast cancer via activation of the epithelial-to-mesenchymal transition
Cytoplasmic granule containing HERMES (显示 CD44 ELISA试剂盒), NonO (显示 NONO ELISA试剂盒), PSF (显示 IL-3 ELISA试剂盒), and G3BP1 is a neuronal RNA-protein granule that is transported in neurites during retinal differentiation.
These results show, for the first time, a requirement for G3BP1 in the control of neuronal plasticity and calcium homeostasis
Data show that protein kinase (显示 CDK7 ELISA试剂盒) R as the principal kinase that mediates eukaryotic initiation factor 2alpha (eIF2alpha (显示 EIF2S1 ELISA试剂盒)) phosphorylation by large RasGAP (显示 RASA1 ELISA试剂盒) SH3-binding protein (显示 SH3BP5 ELISA试剂盒) (G3BP)-induced granules.
Wnt3a-stimulated LRP6 phosphorylation is dependent upon arginine methylation of G3BP2.
arguments against G3BP1 being a genuine RasGAP (显示 RASA1 ELISA试剂盒)-binding partner
G3BP1 is a novel Ctnnb1 (显示 CTNNB1 ELISA试剂盒) mRNA binding protein. Methylation of G3BP1 constitutes a molecular switch that regulates Ctnnb1 (显示 CTNNB1 ELISA试剂盒) mRNA in response to Wnt3a (显示 WNT3A ELISA试剂盒).
It has been demonstrated a depletion of G3BP1 and TIA-1/TIAR in senescent cells and it was shown that the loss of G3BP1 contributed to impaired stress granules formation.
This gene encodes one of the DNA-unwinding enzymes which prefers partially unwound 3'-tailed substrates and can also unwind partial RNA/DNA and RNA/RNA duplexes in an ATP-dependent fashion. This enzyme is a member of the heterogeneous nuclear RNA-binding proteins and is also an element of the Ras signal transduction pathway. It binds specifically to the Ras-GTPase-activating protein by associating with its SH3 domain. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
ras GTPase-activating protein-binding protein 1
, Ras-GTPase-activating protein SH3-domain-binding protein
, GTPase activating protein (SH3 domain) binding protein 1
, ATP-dependent DNA helicase VIII
, GAP SH3 domain-binding protein 1
, GAP binding protein
, RasGAP-associated endoribonuclease G3BP
, ATP-dependent DNA/RNA helicase G3BP
, Ras-GTPase-activating protein SH3-domain binding protein 1
, GAP SH3 binding protein
, GAP SH3 domain-binding protein 2
, Ras-GTPase-activating protein (GAP120) SH3-domain binding protein 2
, Ras-GTPase-activating protein (GAP<120>) SH3-domain binding protein 2
, ras GTPase-activating protein-binding protein 2