1cx7

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(New page: 200px<br /><applet load="1cx7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cx7, resolution 1.94&Aring;" /> '''T4 LYSOZYME METHIONI...)
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[[Image:1cx7.gif|left|200px]]<br /><applet load="1cx7" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1cx7.gif|left|200px]]<br /><applet load="1cx7" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1cx7, resolution 1.94&Aring;" />
caption="1cx7, resolution 1.94&Aring;" />
'''T4 LYSOZYME METHIONINE CORE MUTANT'''<br />
'''T4 LYSOZYME METHIONINE CORE MUTANT'''<br />
==Overview==
==Overview==
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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.
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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==
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1CX7 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=1CX7 OCA].
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1CX7 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=1CX7 OCA].
==Reference==
==Reference==
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[[Category: Lysozyme]]
[[Category: Lysozyme]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Baase, W.A.]]
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[[Category: Baase, W A.]]
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[[Category: Gassner, N.C.]]
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[[Category: Gassner, N C.]]
[[Category: Lindstrom, J.]]
[[Category: Lindstrom, J.]]
[[Category: Lu, J.]]
[[Category: Lu, J.]]
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[[Category: Matthews, B.W.]]
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[[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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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:49:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:10:40 2008''

Revision as of 10:10, 21 February 2008


1cx7, resolution 1.94Å

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T4 LYSOZYME METHIONINE CORE MUTANT

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.

About this Structure

1CX7 is a Single protein structure of sequence from Bacteriophage t4 with and as ligands. Active as Lysozyme, with EC number 3.2.1.17 Full crystallographic information is available from OCA.

Reference

Use of differentially substituted selenomethionine proteins in X-ray structure determination., Gassner NC, Matthews BW, Acta Crystallogr D Biol Crystallogr. 1999 Dec;55(Pt 12):1967-70. PMID:10666571

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