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[[Image:1fl8.gif|left|200px]]


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==HYPERMODIFIED NUCLEOSIDES IN THE ANTICODON OF TRNALYS STABILIZE A CANONICAL U-TURN STRUCTURE==
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<StructureSection load='1fl8' size='340' side='right'caption='[[1fl8]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1fl8]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FL8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1FL8 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PSU:PSEUDOURIDINE-5-MONOPHOSPHATE'>PSU</scene>, <scene name='pdbligand=T6A:N-[N-(9-B-D-RIBOFURANOSYLPURIN-6-YL)CARBAMOYL]THREONINE-5-MONOPHOSPHATE'>T6A</scene>, <scene name='pdbligand=U8U:5-METHYLAMINOMETHYL-2-THIOURIDINE-5-MONOPHOSPHATE'>U8U</scene></td></tr>
{{STRUCTURE_1fl8|  PDB=1fl8  |  SCENE= }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1fl8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fl8 OCA], [https://pdbe.org/1fl8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1fl8 RCSB], [https://www.ebi.ac.uk/pdbsum/1fl8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1fl8 ProSAT]</span></td></tr>
 
</table>
'''HYPERMODIFIED NUCLEOSIDES IN THE ANTICODON OF TRNALYS STABILIZE A CANONICAL U-TURN STRUCTURE'''
<div style="background-color:#fffaf0;">
 
== Publication Abstract from PubMed ==
 
==Overview==
Modified nucleosides in the anticodon domain of Escherichia coli tRNA(Lys) are necessary for high-affinity codon recognition and reading frame maintenance. Human tRNA(Lys,3) is the specific primer for HIV-1 reverse transcriptase and also requires nucleoside modification for proper function. We now present NMR solution structures for the fully modified 17-nucleotide E. coli tRNA(Lys) anticodon stem-loop domain (ASL). NMR data were also collected for several partially modified ASLs, revealing the contributions each modified nucleoside (mnm(5)s(2)U34, t(6)A37, and psi39) makes in transforming the disordered, unmodified tRNA ASL into the highly ordered native structure. The solution structure of the native ASL domain provides insight into longstanding questions regarding both wobble position modification and the nearly ubiquitous t(6)A37 found in tRNAs with an adjacent U at position 36. Native tRNA(Lys) has a U-turn structure similar to the yeast tRNA(Phe) crystal structure, unlike previously proposed "unconventional" anticodon structures characterized by stable interactions between mnm(5)s(2)U-34 and t(6)A-37.
Modified nucleosides in the anticodon domain of Escherichia coli tRNA(Lys) are necessary for high-affinity codon recognition and reading frame maintenance. Human tRNA(Lys,3) is the specific primer for HIV-1 reverse transcriptase and also requires nucleoside modification for proper function. We now present NMR solution structures for the fully modified 17-nucleotide E. coli tRNA(Lys) anticodon stem-loop domain (ASL). NMR data were also collected for several partially modified ASLs, revealing the contributions each modified nucleoside (mnm(5)s(2)U34, t(6)A37, and psi39) makes in transforming the disordered, unmodified tRNA ASL into the highly ordered native structure. The solution structure of the native ASL domain provides insight into longstanding questions regarding both wobble position modification and the nearly ubiquitous t(6)A37 found in tRNAs with an adjacent U at position 36. Native tRNA(Lys) has a U-turn structure similar to the yeast tRNA(Phe) crystal structure, unlike previously proposed "unconventional" anticodon structures characterized by stable interactions between mnm(5)s(2)U-34 and t(6)A-37.


==About this Structure==
Hypermodified nucleosides in the anticodon of tRNALys stabilize a canonical U-turn structure.,Sundaram M, Durant PC, Davis DR Biochemistry. 2000 Oct 17;39(41):12575-84. PMID:11027137<ref>PMID:11027137</ref>
Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FL8 OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Hypermodified nucleosides in the anticodon of tRNALys stabilize a canonical U-turn structure., Sundaram M, Durant PC, Davis DR, Biochemistry. 2000 Oct 17;39(41):12575-84. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11027137 11027137]
</div>
[[Category: Davis, D R.]]
<div class="pdbe-citations 1fl8" style="background-color:#fffaf0;"></div>
[[Category: Durant, P C.]]
== References ==
[[Category: Sundaram, M.]]
<references/>
[[Category: Anticodon]]
__TOC__
[[Category: Mnm5s2u]]
</StructureSection>
[[Category: Pseudouridine]]
[[Category: Large Structures]]
[[Category: T6a]]
[[Category: Davis DR]]
[[Category: Trna]]
[[Category: Durant PC]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 16:27:31 2008''
[[Category: Sundaram M]]
Retrieved from "https://proteopedia.org/1fl8"