期刊
JOURNAL OF STRUCTURAL BIOLOGY
卷 191, 期 1, 页码 10-21出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jsb.2015.06.011
关键词
Guanine nucleotide exchange; Elongation factor Tu; Elongation factor Ts; G-GEF complex; Crystal structure
资金
- Danish Council for Independent Research (Natural Sciences)
- Novo Nordisk Fonden [NNF12OC0002082] Funding Source: researchfish
Translation elongation factor EF-Tu belongs to the superfamily of guanine-nucleotide binding proteins, which play key cellular roles as regulatory switches. All G-proteins require activation via exchange of GDP for GTP to carry out their respective tasks. Often, guanine-nucleotide exchange factors are essential to this process. During translation, EF-Tu:GTP transports aminoacylated tRNA to the ribosome. GTP is hydrolyzed during this process, and subsequent reactivation of EF-Tu is catalyzed by EF-Ts. The reaction path of guanine-nucleotide exchange is structurally poorly defined for EF-Tu and EF-Ts. We have determined the crystal structures of the following reaction intermediates: two structures of EF-Tu:GDP:EF-Ts (2.2 and 1.8 angstrom resolution), EF-Tu:PO4:EF-Ts (1.9 angstrom resolution), EF-Tu:GDPNP:EF-Ts (2.2 angstrom resolution) and EF-Tu:GDPNP:pulvomycin:Mg2+:EF-Ts (3.5 angstrom resolution). These structures provide snapshots throughout the entire exchange reaction and suggest a mechanism for the release of EF-Tu in its GTP conformation. An inferred sequence of events during the exchange reaction is presented. (C) 2015 The Authors. Published by Elsevier Inc.
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