首页> 外文OA文献 >Location of protein S1 of Escherichia coli ribosomes at the 'A'-site of the codon binding site. Affinity labeling studies with a 3'-modified A-U-G analog.
【2h】

Location of protein S1 of Escherichia coli ribosomes at the 'A'-site of the codon binding site. Affinity labeling studies with a 3'-modified A-U-G analog.

机译:大肠杆菌核糖体蛋白S1在密码子结合位点的“ A”位。使用3'-修饰的A-U-G类似物进行亲和标记研究。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

An affinity analog with a 5-bromoacetamido uridine 5'-phosphate moiety bonded to the 3' end of A-U-G has been prepared with the aid of polynucleotide phosphorylase. This 3'-modified, chemically reactive A-U-G analog was used to probe the ribosomal codon binding site. The yield of the reaction depended strongly on the ribosomal source and was sensitive to salt-washing ribosomes. The major crosslinking product was identified to be protein S1. Since the reaction of this 3'-modified A-U-G programmed ribosomes for Met-tRNA-Met-M binding, it is concluded that protein S1 is located at or near the 3'-side of the ribosomal codon binding site.
机译:借助于多核苷酸磷酸化酶已经制备了具有结合到A-U-G的3'末端的5-溴乙酰氨基尿苷5'-磷酸部分的亲和类似物。该3'-修饰的,化学反应性的A-U-G类似物用于探测核糖体密码子结合位点。反应的产率在很大程度上取决于核糖体来源,并且对盐洗核糖体敏感。鉴定出主要的交联产物为蛋白质S1。由于该3'-修饰的A-U-G程序化核糖体对Met-tRNA-Met-M结合的反应,因此可以得出结论,蛋白质S1位于核糖体密码子结合位点的3'侧或附近。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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