期刊
MOLECULAR CELL
卷 52, 期 1, 页码 4-7出版社
CELL PRESS
DOI: 10.1016/j.molcel.2013.09.023
关键词
-
资金
- DFG [Vo875/7-1]
- Bavarian BioSysNet program
Three papers in this issue of Molecular Cell report on the structure and functional activity of type III CRISPR-Cas effector complexes, revealing novel and conserved features of the ribonucleoprotein particles that underlie prokaryotic genome defense. The new structures suggest that type I and type III complexes follow the same architectural principles and are most likely descendants of a common ancestor, the differences in RNA and protein sequences and structure of individual components notwithstanding.
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