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首页> 外文期刊>Antioxidants and redox signalling >The Axonal Motor Neuropathy-Related HINT1 Protein Is a Zinc- and Calmodulin-Regulated Cysteine SUMO Protease
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The Axonal Motor Neuropathy-Related HINT1 Protein Is a Zinc- and Calmodulin-Regulated Cysteine SUMO Protease

机译:轴突电机相关的Hint1蛋白是锌和钙调蛋白调节的半胱氨酸Sumo蛋白酶

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摘要

Histidine triad nucleotide-binding protein 1 (HINT1) exhibits proapoptotic and tumor-suppressive activity. HINT1 binds to transcription factors such as teneurin1 and to the regulator of G protein signaling 17 (RGS) (Z2) protein, which incorporates the small ubiquitin-like modifier (SUMO), and is implicated in several types of cancer. HINT1 interacts with proteins such as PKCγ and Raf-1 through zinc ions provided by the cysteine-rich domain of RGSZ2 and the coupled neural nitric oxide synthase (nNOS). Recently, a series of HINT1 mutants have been reported to cause human autosomal recessive axonal neuropathy with neuromyotonia (ARAN-NM). However, the specific alteration in the function of HINT1 induced by these mutants remains to be elucidated. Because sumoylation modifies protein association and transcriptional regulation, we investigated whether HINT1 exhibits zinc- and redox-regulated sumoylase activity, which may be altered in those mutants.
机译:组氨酸三核苷酸结合蛋白1(Hint1)表现出促凋亡和肿瘤抑制活性。 Hint1与Teneurin1等转录因子结合,并掺入G蛋白信号传导17(RGS)(Z2)蛋白的调节剂,其含有小泛素样改性剂(SUMO),并涉及几种类型的癌症。 Hint1通过由RGSZ2的富含半胱氨酸的致域提供的半胱氨酸域和偶联的神经氮化酶(NNOS)提供的锌离子相互作用。 最近,据报道了一系列致癌突变体导致人常染色体隐性轴心神经病变与神经狭窄(Aran-NM)。 然而,这些突变体诱导的Hint1功能的特异性改变仍然待阐明。 因为Sumoylation改变蛋白质结合和转录调节,所以我们研究了Hint1是否表现出锌和氧化还原调节的苏摩活性,这可以在这些突变体中改变。

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