...
首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >The affected gene underlying the class K glycosyphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase
【24h】

The affected gene underlying the class K glycosyphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase

机译:K类糖基磷脂酰肌醇(GPI)表面蛋白缺陷基础的受影响基因编码GPI转酰胺酶

获取原文
获取原文并翻译 | 示例
           

摘要

The final step in glycosylphosphatidylinosi- tol (GPI) anchoring of cell surface proteins consists of a transamidation reaction in which preassembled GPI donors are substituted for C-terminal signal sequences in nascent polypeptides. In previous studies we described a human K562 cell mutant, termed class K, that accumulates fully assembled GPI units but is unable to transfer them to N-terminally Processed proproteins. In further work we showed that, unlike Wild-type microsomes, microsomes from these cells are unable To support C-terminal interaction of proproteins with the Small nucleophiles hydrazine or hydroxylamine, and that the Cells thus are defective in transamidation.
机译:细胞表面蛋白的糖基磷脂酰肌醇基(GPI)固定的最后一步包括转酰胺基反应,其中预组装的GPI供体被新生多肽中的C端信号序列取代。在先前的研究中,我们描述了一个人类K562细胞突变体,称为K类,该突变体积累了完全组装的GPI单位,但无法将其转移至N末端加工的前蛋白。在进一步的工作中,我们表明,与野生型微粒体不同,来自这些细胞的微粒体无法支持原蛋白与小亲核试剂肼或羟胺的C末端相互作用,因此这些细胞在转酰胺基化方面存在缺陷。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号