2vqe

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{{STRUCTURE_2vqe| PDB=2vqe | SCENE= }}
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'''MODIFIED URIDINES WITH C5-METHYLENE SUBSTITUENTS AT THE FIRST POSITION OF THE TRNA ANTICODON STABILIZE U-G WOBBLE PAIRING DURING DECODING'''
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===MODIFIED URIDINES WITH C5-METHYLENE SUBSTITUENTS AT THE FIRST POSITION OF THE TRNA ANTICODON STABILIZE U-G WOBBLE PAIRING DURING DECODING===
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==Overview==
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Post-transcriptional modifications at the first (wobble) position of the tRNA anticodon participate in precise decoding of the genetic code. To decode codons that end in a purine (R) (i.e. NNR), tRNAs frequently utilize 5-methyluridine derivatives (xm5U) at the wobble position. However, the functional properties of the C5-substituents of xm5U in codon recognition remain elusive. We previously found that mitochondrial tRNAsLeu(UUR) with pathogenic point mutations isolated from MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) patients lacked the 5-taurinomethyluridine (tm5U) modification and caused a decoding defect. To investigate the decoding properties of xm5U modifications related to the molecular pathogenesis of human disease, we constructed E. coli tRNAsLeu(UUR) with or without xm5U modifications at the wobble position, and measured their decoding activities in an in vitro translation as well as by A-site tRNA binding. In addition, the decoding properties of tRNAArg lacking mnm5U modification in a knockout strain of the modifying enzyme (mnmE) were examined by pulse-labeling using reporter constructs with consecutive AGR codons. Our results demonstrate that the xm5U modification plays a critical role in decoding NNG codons by stabilizing U*G pairing at the wobble position. Crystal structures of an anticodon stem-loop containing tm5U interacting with a UUA or UUG codon at the ribosomal A site revealed that the tm5U*G basepair does not have classical U*G wobble geometry. These structures provide help to explain how the tm5U modification enables efficient decoding of UUG codons.
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{{ABSTRACT_PUBMED_18456657}}
==About this Structure==
==About this Structure==
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[[Category: Zinc]]
[[Category: Zinc]]
[[Category: Zinc-finger]]
[[Category: Zinc-finger]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu May 22 22:33:34 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 9 10:09:00 2008''

Revision as of 07:09, 9 July 2008

Image:2vqe.png

Template:STRUCTURE 2vqe

MODIFIED URIDINES WITH C5-METHYLENE SUBSTITUENTS AT THE FIRST POSITION OF THE TRNA ANTICODON STABILIZE U-G WOBBLE PAIRING DURING DECODING

Template:ABSTRACT PUBMED 18456657

About this Structure

2VQE is a Protein complex structure of sequences from Thermus thermophilus. Full crystallographic information is available from OCA.

Reference

Modified uridines with C5-methylene substituents at the first position of the tRNA anticodon stabilize U.G wobble pairing during decoding., Kurata S, Weixlbaumer A, Ohtsuki T, Shimazaki T, Wada T, Kirino Y, Takai K, Watanabe K, Ramakrishnan V, Suzuki T, J Biol Chem. 2008 May 2;. PMID:18456657

Page seeded by OCA on Wed Jul 9 10:09:00 2008

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