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| {{STRUCTURE_2gho| PDB=2gho | SCENE= }} | | {{STRUCTURE_2gho| PDB=2gho | SCENE= }} |
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- | '''Recombinant Thermus aquaticus RNA polymerase for Structural Studies'''
| + | ===Recombinant Thermus aquaticus RNA polymerase for Structural Studies=== |
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- | ==Overview==
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- | Advances in the structural biology of bacterial transcription have come from studies of RNA polymerases (RNAPs) from the thermophilic eubacteria Thermus aquaticus (Taq) and Thermus thermophilus (Tth). These structural studies have been limited by the fact that only endogenous Taq or Tth RNAP, laboriously purified from large quantities of Taq or Tth cell paste and offering few options for genetic modification, is suitable for structural studies. Recombinant systems for the preparation of Taq RNAP by co-overexpression and assembly in the heterologous host, Escherichia coli, have been described, but these did not yield enzyme suitable for crystallographic studies. Here we describe recombinant systems for the preparation of Taq RNAP harboring full or partial deletions of the Taq beta' non-conserved domain (NCD), yielding enzyme suitable for crystallographic studies. This opens the way for structural studies of genetically manipulated enzymes, allowing the preparation of more crystallizable enzymes and facilitating detailed structure/function analysis. Characterization of the Taqbeta'NCD deletion mutants generated in this study showed that the beta'NCD is important for the efficient binding of the sigma subunit, confirming previous hypotheses. Finally, preliminary structural analysis (at 4.1Angstroms resolution) of one of the recombinant mutants revealed a previously unobserved conformation of the beta-flap, further defining the range of conformations accessible to this flexible structural element.
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| + | (as it appears on PubMed at http://www.pubmed.gov), where 16618493 is the PubMed ID number. |
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| + | {{ABSTRACT_PUBMED_16618493}} |
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| ==About this Structure== | | ==About this Structure== |
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| [[Category: Recombinant multiprotein complex]] | | [[Category: Recombinant multiprotein complex]] |
| [[Category: Thermus aquaticus rna polymerase]] | | [[Category: Thermus aquaticus rna polymerase]] |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 05:07:12 2008'' | + | |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 01:12:49 2008'' |
Revision as of 22:12, 27 July 2008
Template:STRUCTURE 2gho
Recombinant Thermus aquaticus RNA polymerase for Structural Studies
Template:ABSTRACT PUBMED 16618493
About this Structure
2GHO is a Protein complex structure of sequences from Thermus aquaticus. Full crystallographic information is available from OCA.
Reference
Recombinant Thermus aquaticus RNA polymerase for structural studies., Kuznedelov K, Lamour V, Patikoglou G, Chlenov M, Darst SA, Severinov K, J Mol Biol. 2006 May 26;359(1):110-21. Epub 2006 Mar 23. PMID:16618493
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