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Solution structure of a SRP19 binding domain in human SRP RNA
被引:17
作者:
Sakamoto, T
Morita, S
Tabata, K
Nakamura, K
Kawai, G
机构:
[1] Chiba Inst Technol, Dept Ind Chem, Fac Engn, Narashino, Chiba 2750016, Japan
[2] Univ Tsukuba, Inst Biol Sci, Tsukuba, Ibaraki 3058572, Japan
[3] RIKEN, Yokohama Inst, Genom Sci Ctr, Yokohama, Kanagawa 2300045, Japan
关键词:
GNAR motif;
helix;
6;
NMR;
signal recognition particle;
tetraloop;
D O I:
10.1093/oxfordjournals.jbchem.a003207
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Assembly of the human signal recognition particle (SRP) requires SRP19 protein to bind to helices 6 and 8 of SRP RNA. In the present study, structure of a 29-mer RNA composing the SRP19 binding site in helix 6 was determined by NMR spectroscopy. The two A:C mismatches were continuously stacked to each other and formed wobble type A.-C base pairs. The GGAG tetraloop, in helix 6 was found to adopt a similar conformation to that of GNRA tetraloop, suggesting that these tetraloops are included in an extensive new motif GNRR. Compared with the crystal structure of helix 6 in complex with SRP19 determined previously, the GGAG tetraloop in the complex was found to adopt a similar conformation to the free form, although the loop structure becomes more open upon SRP19 binding. Thus, SRP19 is thought to recognize the overall fold of the GGAG loop.
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页码:177 / 182
页数:6
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