Function
Required for assembly and stability of the aminoacyl-tRNA synthase complex. Mediates ubiquitination and degradation of FUBP1, a transcriptional activator of MYC, leading to MYC down-regulation which is required for aveolar type II cell differentiation. Blocks MDM2-mediated ubiquitination and degradation of p53/TP53.
Biological Context
Subcellular Location: Cytoplasm, cytosol; Nucleus
Disease Association: Leukodystrophy, hypomyelinating, 17 (HLD17) : An autosomal recessive neurodevelopmental disorder characterized by atrophy of cerebral cortex, spinal cord and cerebellum, thin corpus callosum, abnormal signals in the basal ganglia, and features suggesting hypo- or demyelination observed on brain imaging. Clinical manifestations include lack of development, absent speech, microcephaly, spasticity, seizures, and contractures. [The disease may be caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human Aminoacyl tRNA synthase complex-interacting multifunctional protein 2 (AIMP2) is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 1-320aa, with N-terminal 6xHis-tagged tag, molecular weight 39.3kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications. Explore more Enzyme proteins →
