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Crystal structure of the C-terminal domain of the ε subunit of human translation initiation factor eIF2B
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作者 Jia Wei Minze Jia +4 位作者 Cheng Zhang Mingzhu Wang Feng Gao Hang Xu Weimin Gong 《Protein & Cell》 SCIE CSCD 2010年第6期595-603,共9页
Eukaryotic translation initiation factor eIF2B,the guanine nucleotide exchange factor(GEF)for eIF2,catalyzes conversion of eIF2·GDP to eIF2·GTP.The eIF2B is composed of five subunits,α,β,γ,δandε,within ... Eukaryotic translation initiation factor eIF2B,the guanine nucleotide exchange factor(GEF)for eIF2,catalyzes conversion of eIF2·GDP to eIF2·GTP.The eIF2B is composed of five subunits,α,β,γ,δandε,within which theεsubunit is responsible for catalyzing the guanine exchange reaction.Here we present the crystal structure of the C-terminal domain of human eIF2Bε(eIF2Bε-CTD)at 2.0-Åresolution.The structure resembles a HEAT motif and three charge-rich areas on its surface can be identified.When compared to yeast eIF2Bε-CTD,one area involves highly conserved AA boxes while the other two are only partially conserved.In addition,the previously reported mutations in human eIF2Bε-CTD,which are related to the loss of the GEF activity and human VWM disease,have been discussed.Based on the structure,most of such mutations tend to destabilize the HEAT motif. 展开更多
关键词 eukaryotic translation initiation factor 2b(eIF2b) guanine nucleotide exchange factor(GEF) crystal structure HEAT motif vanishing white matter(VWM)
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