2eet
From Proteopedia
| Line 1: | Line 1: | ||
[[Image:2eet.gif|left|200px]] | [[Image:2eet.gif|left|200px]] | ||
| - | + | <!-- | |
| - | + | The line below this paragraph, containing "STRUCTURE_2eet", creates the "Structure Box" on the page. | |
| - | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
| - | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
| - | | | + | or leave the SCENE parameter empty for the default display. |
| - | | | + | --> |
| - | + | {{STRUCTURE_2eet| PDB=2eet | SCENE= }} | |
| - | + | ||
| - | + | ||
| - | }} | + | |
'''Guanine Riboswitch A21G, U75C mutant bound to hypoxanthine''' | '''Guanine Riboswitch A21G, U75C mutant bound to hypoxanthine''' | ||
| Line 19: | Line 16: | ||
==About this Structure== | ==About this Structure== | ||
| - | 2EET is a [[Single protein]] structure | + | 2EET is a [[Single protein]] structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2EET OCA]. |
==Reference== | ==Reference== | ||
| Line 27: | Line 24: | ||
[[Category: Edwards, A L.]] | [[Category: Edwards, A L.]] | ||
[[Category: Gilbert, S D.]] | [[Category: Gilbert, S D.]] | ||
| - | [[Category: | + | [[Category: Base triple]] |
| - | [[Category: | + | [[Category: Double helix]] |
| - | [[Category: | + | [[Category: Guanine]] |
| - | [[Category: | + | [[Category: Hypoxanthine]] |
| - | [[Category: | + | [[Category: Mrna]] |
| - | [[Category: | + | [[Category: Riboswitch]] |
| - | [[Category: | + | [[Category: Rna-ligand complex]] |
| - | [[Category: | + | [[Category: Three-way junction]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 02:26:36 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 23:26, 3 May 2008
Guanine Riboswitch A21G, U75C mutant bound to hypoxanthine
Overview
The purine riboswitch is one of a number of mRNA elements commonly found in the 5'-untranslated region capable of controlling expression in a cis-fashion via its ability to directly bind small-molecule metabolites. Extensive biochemical and structural analysis of the nucleobase-binding domain of the riboswitch, referred to as the aptamer domain, has revealed that the mRNA recognizes its cognate ligand using an intricately folded three-way junction motif that completely encapsulates the ligand. High-affinity binding of the purine nucleobase is facilitated by a distal loop-loop interaction that is conserved between both the adenine and guanine riboswitches. To understand the contribution of conserved nucleotides in both the three-way junction and the loop-loop interaction of this RNA, we performed a detailed mutagenic survey of these elements in the context of an adenine-responsive variant of the xpt-pbuX guanine riboswitch from Bacillus subtilis. The varying ability of these mutants to bind ligand as measured by isothermal titration calorimetry uncovered the conserved nucleotides whose identity is required for purine binding. Crystallographic analysis of the bound form of five mutants and chemical probing of their free state demonstrate that the identity of several universally conserved nucleotides is not essential for formation of the RNA-ligand complex but rather for maintaining a binding-competent form of the free RNA. These data show that conservation patterns in riboswitches arise from a combination of formation of the ligand-bound complex, promoting an open form of the free RNA, and participating in the secondary structural switch with the expression platform.
About this Structure
2EET is a Single protein structure. Full crystallographic information is available from OCA.
Reference
Mutational analysis of the purine riboswitch aptamer domain., Gilbert SD, Love CE, Edwards AL, Batey RT, Biochemistry. 2007 Nov 20;46(46):13297-309. Epub 2007 Oct 26. PMID:17960911 Page seeded by OCA on Sun May 4 02:26:36 2008
