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PDBsum entry 4lx5

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dna_rna ligands metals links
RNA PDB id
4lx5

 

 

 

 

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Contents
DNA/RNA
Ligands
29G
Metals
_MG ×4
Waters ×17
PDB id:
4lx5
Name: RNA
Title: X-ray crystal structure of the m6" riboswitch aptamer bound to pyrimido[4,5-d]pyrimidine-2,4-diamine (ppda)
Structure: Mutated adenine riboswitch aptamer. Chain: a. Engineered: yes. Mutation: yes
Source: Synthetic: yes. Vibrio vulnificus. Organism_taxid: 672. Other_details: in vitro transcription
Resolution:
2.13Å     R-factor:   0.202     R-free:   0.257
Authors: M.S.Dunstan,D.Leys
Key ref: C.J.Robinson et al. (2014). Modular riboswitch toolsets for synthetic genetic control in diverse bacterial species. J Am Chem Soc, 136, 10615-10624. PubMed id: 24971878 DOI: 10.1021/ja502873j
Date:
29-Jul-13     Release date:   16-Jul-14    
 Headers
 References

DNA/RNA chain
  G-G-C-U-U-C-A-U-A-U-A-A-U-C-C-G-A-A-U-G-A-U-A-U-G-G-U-U-U-C-G-G-A-G-C-U-U-C-C- 71 bases

 

 
DOI no: 10.1021/ja502873j J Am Chem Soc 136:10615-10624 (2014)
PubMed id: 24971878  
 
 
Modular riboswitch toolsets for synthetic genetic control in diverse bacterial species.
C.J.Robinson, H.A.Vincent, M.C.Wu, P.T.Lowe, M.S.Dunstan, D.Leys, J.Micklefield.
 
  ABSTRACT  
 
Ligand-dependent control of gene expression is essential for gene functional analysis, target validation, protein production, and metabolic engineering. However, the expression tools currently available are difficult to transfer between species and exhibit limited mechanistic diversity. Here we demonstrate how the modular architecture of purine riboswitches can be exploited to develop orthogonal and chimeric switches that are transferable across diverse bacterial species, modulating either transcription or translation, to provide tunable activation or repression of target gene expression, in response to synthetic non-natural effector molecules. Our novel riboswitch-ligand pairings are shown to regulate physiologically important genes required for bacterial motility in Escherichia coli and cell morphology in Bacillus subtilis. These findings are relevant for future gene function studies and antimicrobial target validation, while providing new modular and orthogonal regulatory components for deployment in synthetic biology regimes.
 

 

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