Molecular mechanism of stop codon recognition by eRF1
Molecular mechanism of stop codon recognition by eRF1
批准号:
15570104
负责人:
MURAMATSU Tomonari
金额:
$1.98万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004
中文摘要
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英文摘要
ETF1/eRF1,which has recently been suggested to be a myeloid tumor suppressor gene, codes for the class-I release factor which recognizes an in-frame stop codon in translation termination processes of gene expression. This proteinaceous factor eRF1(eukaryotic release factor 1) recognizes all of the three stop codons, UAA, UGA and UAG, but not the Trp codon UGG. This discrimination must require some conformational changes in the recognition domain of eRF1,because the UGG codon cannot be eliminated if eRF1 recognizes the stop codons by simply binding to A/G as the 2nd letter and A/G the 3rd. To address the mechanism of stop codon recognition, we prepared ^<15>N-labeled and ^<15>N/^<13>C-labeled codon recognition domains, assigned all ^1H^N and ^<15>N resonances of native non-proline back bone residues, and now are analyzing dynamic structure of this domain by NMR spectroscopy.
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The three-dimensional structure of aspergilloglutamic peptidase from Aspergillus niger
黑曲霉谷氨酸肽酶的三维结构
DOI:
--
发表时间:
2004
期刊:
Proceedings of Japan Academy 80(B)
影响因子:
--
作者:
[Hiroshi Sasaki, et al.]
通讯作者:
et al.
Backbone ^1H, ^<13>C, and ^<15>N resonance assignment of the N-terminal domain of human eRF1
人eRF1 N端结构域的主链^1H、^<13>C和^<15>N共振分配
DOI:
--
发表时间:
2004
期刊:
J Biomol NMR 30
影响因子:
--
作者:
[Oda Y, Muramatsu T, Yumoto F, Ito M, Tanokura M]
通讯作者:
Tanokura M
Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
鉴定对大肠杆菌信号肽酶 I 活性重要的精氨酸残基
DOI:
--
发表时间:
2004
期刊:
Biological Chemistry 385
影响因子:
--
作者:
[Yong-Tae Kim, et al.]
通讯作者:
et al.
Yoshifumi Oda, Tomonari Muramatsu, Fumiaki Yumoto, Mie Ito, Masaru Tanokura: "Backbone ^1H, ^<13>C and ^<15>N resonance assignment of the N-terminal domain of human eRF1"Journal of Biomolecular NMR. 印刷中. (2004)
Yoshifumi Oda、Tomonari Muramatsu、Fumiaki Yumoto、Mie Ito、Masaru Tanokura:“人 eRF1 N 末端结构域的主干 ^1H、^13>C 和 ^15>N 共振分配”《生物分子 NMR 杂志》出版。 (2004)
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Analysis of dynamic structure of eukaryotic release factor 1 (eRF1)
真核释放因子1(eRF1)动态结构分析
DOI:
--
发表时间:
2004
期刊:
Bioimades 12
影响因子:
--
作者:
[Tomonari Muramatsu, et al.]
通讯作者:
et al.
共 7 条
Autoprocessing mechanism of SARS-CoV 3CL protease
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批准号:20570115
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.58万
-
财政年份:2008
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负责人:MURAMATSU Tomonari
-
依托单位:
海外基金