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首页> 外文期刊>Acta crystallographica. Section F, Structural biology communications >X-ray crystal structure of human calcium-bound S100A1
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X-ray crystal structure of human calcium-bound S100A1

机译:人类钙结合S100A1的X射线晶体结构

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S100A1 is a member of the S100 family of Ca2+-binding proteins and regulates several cellular processes, including those involved in Ca2+ signaling and cardiac and skeletal muscle function. In Alzheimer's disease, brain S100A1 is overexpressed and gives rise to disease pathologies, making it a potential therapeutic target. The 2.25 angstrom resolution crystal structure of Ca2+-S100A1 is solved here and is compared with the structures of other S100 proteins, most notably S100B, which is a highly homologous S100-family member that is implicated in the progression of malignant melanoma. The observed structural differences in S100A1 versus S100B provide insights regarding target proteinbinding specificity and for targeting these two S100 proteins in human diseases using structure-based drug-design approaches.
机译:S100A1是Ca2 + - 桥接蛋白的S100系列的成员,并调节几种细胞过程,包括参与Ca2 +信号传导和心脏和骨骼肌功能的细胞过程。 在阿尔茨海默病的疾病中,脑S100A1过表达并产生疾病病理,使其成为潜在的治疗目标。 这里解决了2.25埃达-100A1的云分辨率晶体结构,并与其他S100蛋白的结构进行了比较,最典型的S100b是一种高度同源的S100家族构件,其涉及恶性黑色素瘤的进展。 观察到的S100A1与S100B的结构差异提供了关于目标蛋白突出特异性的见解,并使用基于结构的药物设计方法对靶向蛋白蛋白突出特异性的见解,并在人类疾病中靶向这两个S100蛋白。

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