2d18: Difference between revisions

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[[Image:2d18.png|left|200px]]


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==Solution RNA structure of loop region of the HIV-1 dimerization initiation site in the extended-duplex dimer==
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<StructureSection load='2d18' size='340' side='right'caption='[[2d18]]' scene=''>
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== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[2d18]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2D18 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2D18 FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2d18 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2d18 OCA], [https://pdbe.org/2d18 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2d18 RCSB], [https://www.ebi.ac.uk/pdbsum/2d18 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2d18 ProSAT]</span></td></tr>
{{STRUCTURE_2d18|  PDB=2d18  |  SCENE=  }}
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Dimer formation of HIV-1 genomic RNA through its dimerization initiation site (DIS) is crucial to maintaining infectivity. Two types of dimers, the initially generated kissing-loop dimer and the subsequent product of the extended-duplex dimer, are formed in the stem-bulge-stem region with a loop including a self-complementary sequence. NMR chemical shift analysis of a 39mer RNA corresponding to DIS, DIS39, in the kissing-loop and extended-duplex dimers revealed that the three dimensional structures of the stem-bulge-stem region are extremely similar between the two types of dimers. Therefore, we designed two shorter RNA molecules, loop25 and bulge34, corresponding to the loop-stem region and the stem-bulge-stem region of DIS39, respectively. Based upon the chemical shift analysis, the conformation of the loop region of loop25 is identical to that of DIS39 for each of the two types of dimers. The conformation of bulge34 was also found to be the same as that of the corresponding region of DIS39. Thus, we determined the solution structures of loop25 in each of the two types of dimers as well as that of bulge34. Finally, the solution structures of DIS39 in the kissing-loop and extended-duplex dimers were determined by combining the parts of the structures. The solution structures of the two types of dimers were similar to each other in general with a difference found only in the A16 residue. The elucidation of the structures of DIS39 is important to understanding the molecular mechanism of the conformational dynamics of viral RNA molecules.


===Solution RNA structure of loop region of the HIV-1 dimerization initiation site in the extended-duplex dimer===
Solution RNA structures of the HIV-1 dimerization initiation site in the kissing-loop and extended-duplex dimers.,Baba S, Takahashi K, Noguchi S, Takaku H, Koyanagi Y, Yamamoto N, Kawai G J Biochem. 2005 Nov;138(5):583-92. PMID:16272570<ref>PMID:16272570</ref>


 
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
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<references/>
{{ABSTRACT_PUBMED_16272570}}
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</StructureSection>
==About this Structure==
[[Category: Large Structures]]
Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2D18 OCA].
[[Category: Baba S]]
 
[[Category: Kawai G]]
==Reference==
[[Category: Koyanagi Y]]
Solution RNA structures of the HIV-1 dimerization initiation site in the kissing-loop and extended-duplex dimers., Baba S, Takahashi K, Noguchi S, Takaku H, Koyanagi Y, Yamamoto N, Kawai G, J Biochem. 2005 Nov;138(5):583-92. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16272570 16272570]
[[Category: Noguchi S]]
[[Category: Baba, S.]]
[[Category: Takahashi K]]
[[Category: Kawai, G.]]
[[Category: Takaku H]]
[[Category: Koyanagi, Y.]]
[[Category: Yamamoto N]]
[[Category: Noguchi, S.]]
[[Category: Takahashi, K.]]
[[Category: Takaku, H.]]
[[Category: Yamamoto, N.]]
[[Category: Di]]
[[Category: Hiv-1]]
[[Category: Nmr]]
[[Category: Rna]]
[[Category: Structure]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 20:43:01 2008''

Latest revision as of 19:33, 13 December 2023

Solution RNA structure of loop region of the HIV-1 dimerization initiation site in the extended-duplex dimerSolution RNA structure of loop region of the HIV-1 dimerization initiation site in the extended-duplex dimer

Structural highlights

2d18 is a 2 chain structure. Full experimental information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:Solution NMR
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Publication Abstract from PubMed

Dimer formation of HIV-1 genomic RNA through its dimerization initiation site (DIS) is crucial to maintaining infectivity. Two types of dimers, the initially generated kissing-loop dimer and the subsequent product of the extended-duplex dimer, are formed in the stem-bulge-stem region with a loop including a self-complementary sequence. NMR chemical shift analysis of a 39mer RNA corresponding to DIS, DIS39, in the kissing-loop and extended-duplex dimers revealed that the three dimensional structures of the stem-bulge-stem region are extremely similar between the two types of dimers. Therefore, we designed two shorter RNA molecules, loop25 and bulge34, corresponding to the loop-stem region and the stem-bulge-stem region of DIS39, respectively. Based upon the chemical shift analysis, the conformation of the loop region of loop25 is identical to that of DIS39 for each of the two types of dimers. The conformation of bulge34 was also found to be the same as that of the corresponding region of DIS39. Thus, we determined the solution structures of loop25 in each of the two types of dimers as well as that of bulge34. Finally, the solution structures of DIS39 in the kissing-loop and extended-duplex dimers were determined by combining the parts of the structures. The solution structures of the two types of dimers were similar to each other in general with a difference found only in the A16 residue. The elucidation of the structures of DIS39 is important to understanding the molecular mechanism of the conformational dynamics of viral RNA molecules.

Solution RNA structures of the HIV-1 dimerization initiation site in the kissing-loop and extended-duplex dimers.,Baba S, Takahashi K, Noguchi S, Takaku H, Koyanagi Y, Yamamoto N, Kawai G J Biochem. 2005 Nov;138(5):583-92. PMID:16272570[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Baba S, Takahashi K, Noguchi S, Takaku H, Koyanagi Y, Yamamoto N, Kawai G. Solution RNA structures of the HIV-1 dimerization initiation site in the kissing-loop and extended-duplex dimers. J Biochem. 2005 Nov;138(5):583-92. PMID:16272570 doi:138/5/583
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