机构:Univ Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Yusupova, GZ
Yusupov, MM
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机构:Univ Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Yusupov, MM
Cate, JHD
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机构:Univ Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Cate, JHD
Noller, HF
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Univ Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USAUniv Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Noller, HF
[1
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机构:
[1] Univ Calif Santa Cruz, Sinsheimer Labs, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Using X-ray crystallography, we have directly observed the path of mRNA in the 70S ribosome in Fourier difference maps at 7 Angstrom resolution. About 30 nucleotides of the mRNA are wrapped in a groove that encircles the neck of the 30S subunit. The Shine-Dalgarno helix is bound in a large cleft between the head and the back of the platform. At the interface, only about eight nucleotides (-1 to +7), centered on the junction between the A and P codons, are exposed, and bond almost exclusively to 16S rRNA. The mRNA enters the ribosome around position + 13 to + 15, the location of downstream pseudoknots that stimulate -1 translational frame shifting.
机构:
ST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USAST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USA
BHANGU, R
WOLLENZIEN, P
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ST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USAST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USA
机构:
ST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USAST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USA
BHANGU, R
WOLLENZIEN, P
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ST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USAST LOUIS UNIV, MED CTR, EDWARD A DOISY DEPT BIOCHEM & MOLEC BIOL, ST LOUIS, MO 63104 USA