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Myoinformatics report: myosin regulatory light chain paralogs in the human genome

机译:肌信息学报告:人类基因组中的肌球蛋白调节性轻链旁系同源物

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摘要

On-line bioinformatics tools were used to identify and characterize all paralogs (intragenomic homologs) of muscle myosin regulatory light chains in the human genome. The initial search yielded 22 possible paralogs, but careful examination of supporting data eliminated most of these. Five paralogs were clearly identified with the tissue types (skeletal and cardiac muscles, smooth muscle, non-muscle cytoplasm) in which they are expressed. Sequence comparisons and phylogenetic analysis showed early divergence of a common ancestor of smooth muscle and non-muscle paralogs from a common ancestor of skeletal and cardiac muscle paralogs. An unusual sixth human paralog was very similar to the regulatory light chain of “superfast” myosin, which to date has been found only in cat. Finally, a unique and questionable “precursor lymphocyte” paralog was tentatively identified. Three-dimensional structural models of all seven human paralogs were constructed using the known structure of chicken fast skeletal muscle regulatory light chain as a template.
机译:在线生物信息学工具用于鉴定和表征人类基因组中肌肉肌球蛋白调节轻链的所有旁系同源物(整合同源)。最初的搜索产生了22种可能的旁系同源物,但是对支持数据的仔细检查消除了其中的大多数。五个旁系同源物与表达它们的组织类型(骨骼肌和心肌,平滑肌,非肌肉细胞质)清楚地识别。序列比较和系统发育分析表明,平滑肌和非肌肉旁系同源物的共同祖先与骨骼肌和心肌旁系同源物的共同祖先早有分歧。一个不寻常的第六人类旁系同源物非常类似于“超快”肌球蛋白的调节轻链,迄今为止,它仅在猫中被发现。最后,初步确定了一个独特且可疑的“前体淋巴细胞”旁系同源物。使用鸡快速骨骼肌调节轻链的已知结构作为模板,构建所有七个人类旁系同源物的三维结构模型。

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