1d3f: Difference between revisions

New page: left|200px<br /><applet load="1d3f" size="450" color="white" frame="true" align="right" spinBox="true" caption="1d3f, resolution 2.05Å" /> '''N-TERMINAL DOMAIN CO...
 
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[[Image:1d3f.jpg|left|200px]]<br /><applet load="1d3f" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1d3f.jpg|left|200px]]<br /><applet load="1d3f" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1d3f, resolution 2.05&Aring;" />
caption="1d3f, resolution 2.05&Aring;" />
'''N-TERMINAL DOMAIN CORE METHIONINE MUTATION'''<br />
'''N-TERMINAL DOMAIN CORE METHIONINE MUTATION'''<br />


==Overview==
==Overview==
Using heavily methionine-substituted T4 lysozyme as an example, it is, shown how the addition or deletion of a small number of methionines can, simplify the location of selenium sites for use in MAD phasing. By, comparing the X-ray data for a large number of singly substituted, lysozymes, it is shown that the optimal amino acid to be substituted by, methionine is leucine, followed, in order of preference, by phenylalanine, isoleucine and valine. The identification of leucine as the first choice, agrees with the ranking suggested by the Dayhoff mutation probability, i.e. by the frequency of amino-acid substitutions in the sequences of, related proteins. The ranking of the second and subsequent choices, however, differ significantly.
Using heavily methionine-substituted T4 lysozyme as an example, it is shown how the addition or deletion of a small number of methionines can simplify the location of selenium sites for use in MAD phasing. By comparing the X-ray data for a large number of singly substituted lysozymes, it is shown that the optimal amino acid to be substituted by methionine is leucine, followed, in order of preference, by phenylalanine, isoleucine and valine. The identification of leucine as the first choice agrees with the ranking suggested by the Dayhoff mutation probability, i.e. by the frequency of amino-acid substitutions in the sequences of related proteins. The ranking of the second and subsequent choices, however, differ significantly.


==About this Structure==
==About this Structure==
1D3F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteriophage_t4 Bacteriophage t4] with CL and HED as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1D3F OCA].  
1D3F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteriophage_t4 Bacteriophage t4] with <scene name='pdbligand=CL:'>CL</scene> and <scene name='pdbligand=HED:'>HED</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D3F OCA].  


==Reference==
==Reference==
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[[Category: Lysozyme]]
[[Category: Lysozyme]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Gassner, N.C.]]
[[Category: Gassner, N C.]]
[[Category: Matthews, B.W.]]
[[Category: Matthews, B W.]]
[[Category: CL]]
[[Category: CL]]
[[Category: HED]]
[[Category: HED]]
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[[Category: t4 lysozyme]]
[[Category: t4 lysozyme]]


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