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New page: left|200px<br /><applet load="1vbn" size="450" color="white" frame="true" align="right" spinBox="true" caption="1vbn, resolution 2.70Å" /> '''Escherichia coli tyr...
 
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[[Image:1vbn.gif|left|200px]]<br /><applet load="1vbn" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1vbn.gif|left|200px]]<br /><applet load="1vbn" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1vbn, resolution 2.70&Aring;" />
caption="1vbn, resolution 2.70&Aring;" />
'''Escherichia coli tyrosyl-tRNA synthetase mutant complexed with Tyr-AMS'''<br />
'''Escherichia coli tyrosyl-tRNA synthetase mutant complexed with Tyr-AMS'''<br />


==Overview==
==Overview==
The genetic code in a eukaryotic system has been expanded by the, engineering of Escherichia coli tyrosyl-tRNA synthetase (TyrRS) with the, Y37V and Q195C mutations (37V195C), which specifically recognize, 3-iodo-L-tyrosine rather than L-tyrosine. In the present study, we, determined the 3-iodo-L-tyrosine- and L-tyrosine-bound structures of the, 37V195C mutant of the E. coli TyrRS catalytic domain at 2.0-A resolution., The gamma-methyl group of Val-37 and the sulfur atom of Cys-195 make van, der Waals contacts with the iodine atom of 3-iodo-L-tyrosine. The Val-37, and Cys-195 side chains are rigidly fixed by the neighboring residues, forming the hydrophobic core of the TyrRS. The major roles of the two, mutations are different for the 3-iodo-L-tyrosine-selective recognition in, the first step of the aminoacylation reaction (the amino acid activation, step): the Y37V mutation eliminates the fatal steric repulsion with the, iodine atom, and the Q195C mutation reduces the L-tyrosine misrecognition., The structure of the 37V195C mutant TyrRS complexed with an, L-tyrosyladenylate analogue was also solved, indicating that the, 3-iodo-L-tyrosine and L-tyrosine side chains are similarly discriminated, in the second step (the aminoacyl transfer step). These results, demonstrate that the amino acid-binding pocket on the 37V195C mutant is, optimized for specific 3-iodo-L-tyrosine recognition.
The genetic code in a eukaryotic system has been expanded by the engineering of Escherichia coli tyrosyl-tRNA synthetase (TyrRS) with the Y37V and Q195C mutations (37V195C), which specifically recognize 3-iodo-L-tyrosine rather than L-tyrosine. In the present study, we determined the 3-iodo-L-tyrosine- and L-tyrosine-bound structures of the 37V195C mutant of the E. coli TyrRS catalytic domain at 2.0-A resolution. The gamma-methyl group of Val-37 and the sulfur atom of Cys-195 make van der Waals contacts with the iodine atom of 3-iodo-L-tyrosine. The Val-37 and Cys-195 side chains are rigidly fixed by the neighboring residues forming the hydrophobic core of the TyrRS. The major roles of the two mutations are different for the 3-iodo-L-tyrosine-selective recognition in the first step of the aminoacylation reaction (the amino acid activation step): the Y37V mutation eliminates the fatal steric repulsion with the iodine atom, and the Q195C mutation reduces the L-tyrosine misrecognition. The structure of the 37V195C mutant TyrRS complexed with an L-tyrosyladenylate analogue was also solved, indicating that the 3-iodo-L-tyrosine and L-tyrosine side chains are similarly discriminated in the second step (the aminoacyl transfer step). These results demonstrate that the amino acid-binding pocket on the 37V195C mutant is optimized for specific 3-iodo-L-tyrosine recognition.


==About this Structure==
==About this Structure==
1VBN is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with YSA as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Tyrosine--tRNA_ligase Tyrosine--tRNA ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.1.1.1 6.1.1.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1VBN OCA].  
1VBN is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=YSA:'>YSA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Tyrosine--tRNA_ligase Tyrosine--tRNA ligase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.1.1.1 6.1.1.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VBN OCA].  


==Reference==
==Reference==
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[[Category: Kobayashi, T.]]
[[Category: Kobayashi, T.]]
[[Category: Nishimura, S.]]
[[Category: Nishimura, S.]]
[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Sakamoto, K.]]
[[Category: Sakamoto, K.]]
[[Category: Sekine, R.]]
[[Category: Sekine, R.]]
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[[Category: structural genomics]]
[[Category: structural genomics]]


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