期刊
CELL
卷 107, 期 3, 页码 373-386出版社
CELL PRESS
DOI: 10.1016/S0092-8674(01)00539-6
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资金
- NCRR NIH HHS [P41 RR01219] Funding Source: Medline
- NIGMS NIH HHS [R01 GM60635, R37 GM29169, GM 54762] Funding Source: Medline
A cryo-EM reconstruction of the translating yeast 80S ribosome was analyzed. Computationally separated rRNA and protein densities were used for docking of appropriately modified rRNA models and homology models of yeast ribosomal proteins. The core of the ribosome shows a remarkable degree of conservation. However, some significant differences in functionally important regions and dramatic changes in the periphery due to expansion segments and additional ribosomal proteins are evident. As in the bacterial ribosome, bridges between the subunits are mainly formed by RNA contacts. Four new bridges are present at the periphery. The position of the P site tRNA coincides precisely with its prokaryotic counterpart, with mainly rRNA contributing to its molecular environment. This analysis presents an exhaustive inventory of an eukaryotic ribosome at the molecular level.
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