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清华-富士康纳米科技前沿论坛(第十六讲):基于硫系相变材料的光子存储与光子计算
AIR学术沙龙第24期 | 微软副总裁高剑峰:Brain-inspired Efficient AI modeling
New paradigms of photonic state manipulation on synthetic platforms
清华-富士康纳米科技前沿论坛(第十五讲): 通道蛋白的功能仿生
报告题目:
Structural basis of genetic code translation
 报告人:
Osamu Nureki
Dept. of Biological Information,Tokyo Institute of Technology, Japan
报告时间:
2006-04-24 10:00
报告地点:
化学工程系(工物馆)324东会议室
主办单位:
化学工程系
  简介:

Transfer RNA (tRNA) is a key molecule to decode the genetic information on mRNA to amino acids (protein) in a ribosome.  For tRNA to fulfill its adaptor function, tRNA should be processed into the standard length, post-transcriptionally modified, and aminoacylated (tRNA maturation steps) by the relevant enzymes with excellent substrate specificity.  Especially, the modification step is essential for the tRNA to maintain the canonical L-shaped structure, to ensure the correct codon-anticodon pairing, and to be specifically recognized by the cognate aaRS, which is required for the decoding function of tRNA.  Recent genome analyses and post-genome (proteomics and ribonucleomics) analyses have identified genes involved in the tRNA processing, modification, and aminoacylation.  Furthermore, post-genomic structural analysis has elucidated the structural basis for the tRNA maturation mechanism.  Here we present our recent progress of the structural biology of the tRNA maturation.

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