首页> 外文期刊>Journal of pharmacological sciences. >Molecular Mechanisms and Drug Development in Aquaporin Water Channel Diseases: Aquaporin Superfamily (Superaquaporins): Expansion of Aquaporins Restricted to Multicellular Organisms.
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Molecular Mechanisms and Drug Development in Aquaporin Water Channel Diseases: Aquaporin Superfamily (Superaquaporins): Expansion of Aquaporins Restricted to Multicellular Organisms.

机译:水通道蛋白水通道疾病的分子机制和药物开发:水通道蛋白超家族(Superaquaporins):水通道蛋白的扩展仅限于多细胞生物。

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摘要

Eleven aquaporins are identified in mammals. They all have highly conserved two asparagine-proline-alanine (NPA) boxes that are important for the formation of the water permeating pore. Recently we identified two new proteins in mammals distantly related to aquaporins (AQPs) with poorly conserved NPA boxes. Similarly poorly conserved AQP-like proteins were found in several genome projects of multicellular organisms. They may be subgrouped as the AQP superfamily or superaquaporins. Their function is still unknown. AQP11 knockout mice suffer from polycystic kidneys and neonatal fatality. The identification of superaquaporins will provide new insights into the role of AQPs in organogenesis.
机译:在哺乳动物中鉴定出十一种水通道蛋白。它们都具有高度保守的两个天冬酰胺-脯氨酸-丙氨酸(NPA)盒,这对于形成水渗透孔非常重要。最近,我们在保守性差的NPA盒中发现了与水通道蛋白(AQPs)远缘的哺乳动物中的两种新蛋白。同样,在多细胞生物的几个基因组计划中也发现了保守性差的AQP样蛋白。它们可以分为AQP超家族或超水通道蛋白。它们的功能仍然未知。 AQP11基因敲除小鼠患有多囊肾和新生儿死亡。超级水通道蛋白的鉴定将提供有关AQP在器官发生中作用的新见解。

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