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1q74

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(New page: 200px<br /><applet load="1q74" size="450" color="white" frame="true" align="right" spinBox="true" caption="1q74, resolution 1.70&Aring;" /> '''The Crystal Structur...)
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[[Image:1q74.gif|left|200px]]<br /><applet load="1q74" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1q74.gif|left|200px]]<br /><applet load="1q74" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1q74, resolution 1.70&Aring;" />
caption="1q74, resolution 1.70&Aring;" />
'''The Crystal Structure of 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside Deacetylase (MshB)'''<br />
'''The Crystal Structure of 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside Deacetylase (MshB)'''<br />
==Overview==
==Overview==
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The C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane, 1,3-dioxide, was found to react with a range of 3-oxidopyridinium betaines, (bearing different substituents on nitrogen) in high yield and with total, diastereoselectivity. A 2.3:1 mixture of regioisomers was formed with all, of the 3-oxidopyridinium betaines but the ratio was found to change over, prolonged periods of time due to reversibility of the minor regioisomer., 3-Oxidopyridinium betaines bearing methyl substituents at either the 2- or, 6-position were also tested in the cycloaddition process. Improved, regioselectivity (8:1) and again high diastereoselectivity were observed, with the betaine having an additional substituent at the 2-position, but, with betaines having a substituent in the 6-position although high, regioselectivity was observed (9.9:1), the major isomer was formed with, low diastereoselectivity (5.5:4.4). The origin of the regio- and, diastereo-selectivity with all the betaines is discussed. Finally, the, C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane 1,3-dioxide, was reacted with an oxidopyrylium betaine in moderate yield. Good, regioselectivity and moderate diastereoselectivity were observed.
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The C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane 1,3-dioxide, was found to react with a range of 3-oxidopyridinium betaines (bearing different substituents on nitrogen) in high yield and with total diastereoselectivity. A 2.3:1 mixture of regioisomers was formed with all of the 3-oxidopyridinium betaines but the ratio was found to change over prolonged periods of time due to reversibility of the minor regioisomer. 3-Oxidopyridinium betaines bearing methyl substituents at either the 2- or 6-position were also tested in the cycloaddition process. Improved regioselectivity (8:1) and again high diastereoselectivity were observed with the betaine having an additional substituent at the 2-position, but with betaines having a substituent in the 6-position although high regioselectivity was observed (9.9:1), the major isomer was formed with low diastereoselectivity (5.5:4.4). The origin of the regio- and diastereo-selectivity with all the betaines is discussed. Finally, the C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane 1,3-dioxide was reacted with an oxidopyrylium betaine in moderate yield. Good regioselectivity and moderate diastereoselectivity were observed.
==About this Structure==
==About this Structure==
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1Q74 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with ZN and PE4 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Q74 OCA].
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1Q74 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=PE4:'>PE4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Q74 OCA].
==Reference==
==Reference==
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[[Category: Arad, D.]]
[[Category: Arad, D.]]
[[Category: Av-Gay, Y.]]
[[Category: Av-Gay, Y.]]
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[[Category: Cherney, M.M.]]
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[[Category: Cherney, M M.]]
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[[Category: Fahey, R.C.]]
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[[Category: Fahey, R C.]]
[[Category: Garen, C.]]
[[Category: Garen, C.]]
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[[Category: James, M.N.]]
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[[Category: James, M N.]]
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[[Category: Maynes, J.T.]]
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[[Category: Maynes, J T.]]
[[Category: Newton, G.]]
[[Category: Newton, G.]]
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[[Category: TBSGC, TB.Structural.Genomics.Consortium.]]
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[[Category: TBSGC, TB Structural Genomics Consortium.]]
[[Category: PE4]]
[[Category: PE4]]
[[Category: ZN]]
[[Category: ZN]]
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[[Category: zinc aminohydrolase]]
[[Category: zinc aminohydrolase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 03:40:23 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:36:34 2008''

Revision as of 12:36, 21 February 2008


1q74, resolution 1.70Å

Drag the structure with the mouse to rotate

The Crystal Structure of 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside Deacetylase (MshB)

Overview

The C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane 1,3-dioxide, was found to react with a range of 3-oxidopyridinium betaines (bearing different substituents on nitrogen) in high yield and with total diastereoselectivity. A 2.3:1 mixture of regioisomers was formed with all of the 3-oxidopyridinium betaines but the ratio was found to change over prolonged periods of time due to reversibility of the minor regioisomer. 3-Oxidopyridinium betaines bearing methyl substituents at either the 2- or 6-position were also tested in the cycloaddition process. Improved regioselectivity (8:1) and again high diastereoselectivity were observed with the betaine having an additional substituent at the 2-position, but with betaines having a substituent in the 6-position although high regioselectivity was observed (9.9:1), the major isomer was formed with low diastereoselectivity (5.5:4.4). The origin of the regio- and diastereo-selectivity with all the betaines is discussed. Finally, the C2-symmetric vinyl sulfoxide, trans-2-methylene-1,3-dithiolane 1,3-dioxide was reacted with an oxidopyrylium betaine in moderate yield. Good regioselectivity and moderate diastereoselectivity were observed.

About this Structure

1Q74 is a Single protein structure of sequence from Mycobacterium tuberculosis with and as ligands. Full crystallographic information is available from OCA.

Reference

Highly diastereoselective 1,3-dipolar cycloaddition reactions of trans-2-methylene-1,3-dithiolane 1,3-dioxide with 3-oxidopyridinium and 3-oxidopyrylium betaines: a route to the tropane skeleton., Aggarwal VK, Grainger RS, Newton GK, Spargo PL, Hobson AD, Adams H, Org Biomol Chem. 2003 Jun 7;1(11):1884-93. PMID:12945769

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