2a12: Difference between revisions
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==THEORETICAL MODEL OF THE AI5G GROUP II INTRON== | |||
<StructureSection load='2a12' size='340' side='right' caption='[[2a12]]' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2A12 FirstGlance]. <br> | |||
</td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2a12 FirstGlance], [http://www.ebi.ac.uk/pdbsum/2a12 PDBsum]</span></td></tr> | |||
<table> | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Despite the biological importance of self-splicing group II introns, little is known about their structural organization. Synthetic incorporation of site-specific photo-cross-linkers within catalytic domains resulted in functional distance constraints that, when combined with known tertiary interactions, provide a three-dimensional view of the active intron architecture. All functionalities important for both steps of splicing are proximal before the first step, suggestive of a single active-site region for group II intron catalysis. | |||
A single active-site region for a group II intron.,de Lencastre A, Hamill S, Pyle AM Nat Struct Mol Biol. 2005 Jul;12(7):626-7. Epub 2005 Jun 26. PMID:15980867<ref>PMID:15980867</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
== | |||
< | |||
[[Category: De Lencastre, A]] | [[Category: De Lencastre, A]] | ||
[[Category: Hamill, S]] | [[Category: Hamill, S]] | ||
[[Category: Pyle, A M]] | [[Category: Pyle, A M]] | ||
Revision as of 00:54, 2 October 2014
THEORETICAL MODEL OF THE AI5G GROUP II INTRON
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