3la5: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:


==X-ray crystal structure of mc6 RNA Riboswitch bound to azacytosine==
==X-ray crystal structure of mc6 RNA Riboswitch bound to azacytosine==
<StructureSection load='3la5' size='340' side='right' caption='[[3la5]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
<StructureSection load='3la5' size='340' side='right'caption='[[3la5]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[3la5]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3LA5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3LA5 FirstGlance]. <br>
<table><tr><td colspan='2'>[[3la5]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3LA5 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=3LA5 FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5AZ:6-AMINO-1,3,5-TRIAZIN-2(1H)-ONE'>5AZ</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=5AZ:6-AMINO-1,3,5-TRIAZIN-2(1H)-ONE'>5AZ</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1y26|1y26]]</td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1y26|1y26]]</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3la5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3la5 OCA], [http://pdbe.org/3la5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3la5 RCSB], [http://www.ebi.ac.uk/pdbsum/3la5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3la5 ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=3la5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3la5 OCA], [http://pdbe.org/3la5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3la5 RCSB], [http://www.ebi.ac.uk/pdbsum/3la5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3la5 ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
Line 19: Line 19:


==See Also==
==See Also==
*[[Riboswitch|Riboswitch]]
*[[Riboswitch 3D structures|Riboswitch 3D structures]]
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Dunstan, M S]]
[[Category: Dunstan, M S]]
[[Category: Leys, D]]
[[Category: Leys, D]]

Revision as of 10:05, 7 October 2020

X-ray crystal structure of mc6 RNA Riboswitch bound to azacytosineX-ray crystal structure of mc6 RNA Riboswitch bound to azacytosine

Structural highlights

3la5 is a 1 chain structure. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Publication Abstract from PubMed

The ability to independently control the expression of multiple genes by addition of distinct small-molecule modulators has many applications from synthetic biology, functional genomics, pharmaceutical target validation, through to gene therapy. Riboswitches are relatively simple, small-molecule-dependent, protein-free, mRNA genetic switches that are attractive targets for reengineering in this context. Using a combination of chemical genetics and genetic selection, we have developed riboswitches that are selective for synthetic "nonnatural" small molecules and no longer respond to the natural intracellular ligands. The orthogonal selectivity of the riboswitches is also demonstrated in vitro using isothermal titration calorimetry and x-ray crystallography. The riboswitches allow highly responsive, dose-dependent, orthogonally selective, and dynamic control of gene expression in vivo. It is possible that this approach may be further developed to reengineer other natural riboswitches for application as small-molecule responsive genetic switches in both prokaryotes and eukaryotes.

Reengineering orthogonally selective riboswitches.,Dixon N, Duncan JN, Geerlings T, Dunstan MS, McCarthy JE, Leys D, Micklefield J Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2830-5. Epub 2010 Jan 26. PMID:20133756[1]

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

See Also

References

  1. Dixon N, Duncan JN, Geerlings T, Dunstan MS, McCarthy JE, Leys D, Micklefield J. Reengineering orthogonally selective riboswitches. Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2830-5. Epub 2010 Jan 26. PMID:20133756

3la5, resolution 1.70Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA