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New page: left|200px<br /><applet load="1vfg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1vfg, resolution 2.8Å" /> '''Crystal structure of ...
 
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[[Image:1vfg.gif|left|200px]]<br /><applet load="1vfg" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1vfg.gif|left|200px]]<br /><applet load="1vfg" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1vfg, resolution 2.8&Aring;" />
caption="1vfg, resolution 2.8&Aring;" />
'''Crystal structure of tRNA nucleotidyltransferase complexed with a primer tRNA and an incoming ATP analog'''<br />
'''Crystal structure of tRNA nucleotidyltransferase complexed with a primer tRNA and an incoming ATP analog'''<br />


==Overview==
==Overview==
The 3'-terminal CCA nucleotide sequence (positions 74-76) of transfer RNA, is essential for amino acid attachment and interaction with the ribosome, during protein synthesis. The CCA sequence is synthesized de novo and/or, repaired by a template-independent RNA polymerase, 'CCA-adding enzyme', using CTP and ATP as substrates. Despite structural and biochemical, studies, the mechanism by which the CCA-adding enzyme synthesizes the, defined sequence without a nucleic acid template remains elusive. Here we, present the crystal structure of Aquifex aeolicus CCA-adding enzyme, bound, to a primer tRNA lacking the terminal adenosine and an incoming ATP, analogue, at 2.8 A resolution. The enzyme enfolds the acceptor T helix of, the tRNA molecule. In the catalytic pocket, C75 is adjacent to ATP, and, their base moieties are stacked. The complementary pocket for recognizing, C74-C75 of tRNA forms a 'protein template' for the penultimate two, nucleotides, mimicking the nucleotide template used by template-dependent, polymerases. These results are supported by systematic analyses of, mutants. Our structure represents the 'pre-insertion' stage of selecting, the incoming nucleotide and provides the structural basis for the, mechanism underlying template-independent RNA polymerization.
The 3'-terminal CCA nucleotide sequence (positions 74-76) of transfer RNA is essential for amino acid attachment and interaction with the ribosome during protein synthesis. The CCA sequence is synthesized de novo and/or repaired by a template-independent RNA polymerase, 'CCA-adding enzyme', using CTP and ATP as substrates. Despite structural and biochemical studies, the mechanism by which the CCA-adding enzyme synthesizes the defined sequence without a nucleic acid template remains elusive. Here we present the crystal structure of Aquifex aeolicus CCA-adding enzyme, bound to a primer tRNA lacking the terminal adenosine and an incoming ATP analogue, at 2.8 A resolution. The enzyme enfolds the acceptor T helix of the tRNA molecule. In the catalytic pocket, C75 is adjacent to ATP, and their base moieties are stacked. The complementary pocket for recognizing C74-C75 of tRNA forms a 'protein template' for the penultimate two nucleotides, mimicking the nucleotide template used by template-dependent polymerases. These results are supported by systematic analyses of mutants. Our structure represents the 'pre-insertion' stage of selecting the incoming nucleotide and provides the structural basis for the mechanism underlying template-independent RNA polymerization.


==About this Structure==
==About this Structure==
1VFG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aquifex_aeolicus Aquifex aeolicus] with APC as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Polynucleotide_adenylyltransferase Polynucleotide adenylyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.19 2.7.7.19] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1VFG OCA].  
1VFG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aquifex_aeolicus Aquifex aeolicus] with <scene name='pdbligand=APC:'>APC</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Polynucleotide_adenylyltransferase Polynucleotide adenylyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.19 2.7.7.19] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VFG OCA].  


==Reference==
==Reference==
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[[Category: Ishitani, R.]]
[[Category: Ishitani, R.]]
[[Category: Nureki, O.]]
[[Category: Nureki, O.]]
[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Takeuchi, N.]]
[[Category: Takeuchi, N.]]
[[Category: Tomita, K.]]
[[Category: Tomita, K.]]
[[Category: Ueda, T.]]
[[Category: Ueda, T.]]
[[Category: Vassylyev, D.G.]]
[[Category: Vassylyev, D G.]]
[[Category: APC]]
[[Category: APC]]
[[Category: riken structural genomics/proteomics initiative]]
[[Category: riken structural genomics/proteomics initiative]]
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[[Category: transferase]]
[[Category: transferase]]


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