Recombinant Human Smg1 protein
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Recombinant Human Smg1 protein is a Human Fragment protein, in the 2922 to 3031 aa range, expressed in Wheat germ, suitable for ELISA, WB.
View Alternative Names
ATX, KIAA0421, LIP, SMG1, Serine/threonine-protein kinase SMG1, SMG-1, hSMG-1, Lambda/iota protein kinase C-interacting protein, Nonsense mediated mRNA decay-associated PI3K-related kinase SMG1, Lambda-interacting protein
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human Smg1 protein (AB161516)
ab161516 on a 12.5% SDS-PAGE stained with Coomassie Blue.
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Smg1 plays an important part in the nonsense-mediated mRNA decay (NMD) pathway an important cellular process for RNA surveillance mechanisms. Smg1 associates with other proteins forming a complex known as the SMG1C complex which monitors and degrades faulty mRNAs that contain premature stop codons to prevent the production of truncated proteins. Smg1 aids in safeguarding the cellular transcriptome integrity by ensuring quality control at the mRNA level.
Pathways
Smg1 interacts importantly within the NMD pathway alongside proteins UPF1 and UPF2 which are essential for proper function. Smg1 is also involved in the cellular response to stress pathways contributing to the regulation of stress granules. Through these pathways Smg1 ensures proper adaptation and response to changing cellular conditions maintaining overall cell health and functionality.
Specifications
Form
Liquid
General info
Function
Serine/threonine protein kinase involved in both mRNA surveillance and genotoxic stress response pathways. Recognizes the substrate consensus sequence [ST]-Q. Plays a central role in nonsense-mediated decay (NMD) of mRNAs containing premature stop codons by phosphorylating UPF1/RENT1. Recruited by release factors to stalled ribosomes together with SMG8 and SMG9 (forming the SMG1C protein kinase complex), and UPF1 to form the transient SURF (SMG1-UPF1-eRF1-eRF3) complex. In EJC-dependent NMD, the SURF complex associates with the exon junction complex (EJC) through UPF2 and allows the formation of an UPF1-UPF2-UPF3 surveillance complex which is believed to activate NMD. Also acts as a genotoxic stress-activated protein kinase that displays some functional overlap with ATM. Can phosphorylate p53/TP53 and is required for optimal p53/TP53 activation after cellular exposure to genotoxic stress. Its depletion leads to spontaneous DNA damage and increased sensitivity to ionizing radiation (IR). May activate PRKCI but not PRKCZ.
Sequence similarities
Belongs to the PI3/PI4-kinase family.
Post-translational modifications
Autophosphorylated.
Subcellular localisation
Nucleus
Target data
Product promise
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