1sii: Difference between revisions

New page: left|200px<br /><applet load="1sii" size="450" color="white" frame="true" align="right" spinBox="true" caption="1sii, resolution 1.70Å" /> '''AGAO in covalent com...
 
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[[Image:1sii.gif|left|200px]]<br /><applet load="1sii" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1sii.gif|left|200px]]<br /><applet load="1sii" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1sii, resolution 1.70&Aring;" />
caption="1sii, resolution 1.70&Aring;" />
'''AGAO in covalent complex with the inhibitor NOBA ("4-(2-naphthyloxy)-2-butyn-1-amine")'''<br />
'''AGAO in covalent complex with the inhibitor NOBA ("4-(2-naphthyloxy)-2-butyn-1-amine")'''<br />


==Overview==
==Overview==
A series of compounds derived from a previously identified substrate, analogue of copper amine oxidases (CuAOs) (Shepard et al. (2002) Eur. J., Biochem. 269, 3645-3658) has been screened against six different CuAOs, with a view to designing potent and selective inhibitors. The substrate, analogues investigated were 4-(1-naphthyloxy)-2-butyn-1-amine, 4-(2-methylphenoxy)-2-butyn-1-amine, 4-(3-methylphenoxy)-2-butyn-1-amine, 4-(4-methylphenoxy)-2-butyn-1-amine, and 4-phenoxy-2-butyn-1-amine. These, compounds were screened against equine plasma amine oxidase (EPAO), Pisum, sativum amine oxidase (PSAO), Pichia pastoris lysyl oxidase (PPLO), bovine, plasma amine oxidase (BPAO), human kidney diamine oxidase (KDAO), and, Arthrobacter globiformis amine oxidase (AGAO) to examine the effect of, different substituent groups on potency. Despite the similar structures of, the 4-aryloxy analogues evaluated, striking differences in potency were, observed. In addition, crystal structures of AGAO derivitized with, 4-(2-naphthyloxy)-2-butyn-1-amine and 4-(4-methylphenoxy)-2-butyn-1-amine, were obtained at a resolution of 1.7 A. The structures reveal a novel and, unprecedented reaction mechanism involving covalent attachment of the, alpha,beta-unsaturated aldehyde turnover product to the amino group of the, reduced 2,4,5-trihydroxyphenylalanine quinone (TPQ) cofactor., Collectively, the structural and inhibition results support the, feasibility of designing selective mechanism-based inhibitors of copper, amine oxidases.
A series of compounds derived from a previously identified substrate analogue of copper amine oxidases (CuAOs) (Shepard et al. (2002) Eur. J. Biochem. 269, 3645-3658) has been screened against six different CuAOs with a view to designing potent and selective inhibitors. The substrate analogues investigated were 4-(1-naphthyloxy)-2-butyn-1-amine, 4-(2-methylphenoxy)-2-butyn-1-amine, 4-(3-methylphenoxy)-2-butyn-1-amine, 4-(4-methylphenoxy)-2-butyn-1-amine, and 4-phenoxy-2-butyn-1-amine. These compounds were screened against equine plasma amine oxidase (EPAO), Pisum sativum amine oxidase (PSAO), Pichia pastoris lysyl oxidase (PPLO), bovine plasma amine oxidase (BPAO), human kidney diamine oxidase (KDAO), and Arthrobacter globiformis amine oxidase (AGAO) to examine the effect of different substituent groups on potency. Despite the similar structures of the 4-aryloxy analogues evaluated, striking differences in potency were observed. In addition, crystal structures of AGAO derivitized with 4-(2-naphthyloxy)-2-butyn-1-amine and 4-(4-methylphenoxy)-2-butyn-1-amine were obtained at a resolution of 1.7 A. The structures reveal a novel and unprecedented reaction mechanism involving covalent attachment of the alpha,beta-unsaturated aldehyde turnover product to the amino group of the reduced 2,4,5-trihydroxyphenylalanine quinone (TPQ) cofactor. Collectively, the structural and inhibition results support the feasibility of designing selective mechanism-based inhibitors of copper amine oxidases.


==About this Structure==
==About this Structure==
1SII is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Arthrobacter_globiformis Arthrobacter globiformis] with CU, NA, SO4 and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Amine_oxidase_(copper-containing) Amine oxidase (copper-containing)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.6 1.4.3.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SII OCA].  
1SII is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Arthrobacter_globiformis Arthrobacter globiformis] with <scene name='pdbligand=CU:'>CU</scene>, <scene name='pdbligand=NA:'>NA</scene>, <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Amine_oxidase_(copper-containing) Amine oxidase (copper-containing)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.6 1.4.3.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SII OCA].  


==Reference==
==Reference==
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[[Category: Arthrobacter globiformis]]
[[Category: Arthrobacter globiformis]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Duff, A.P.]]
[[Category: Duff, A P.]]
[[Category: Guss, J.M.]]
[[Category: Guss, J M.]]
[[Category: Langley, D.B.]]
[[Category: Langley, D B.]]
[[Category: CU]]
[[Category: CU]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: trihydroxyphenylalanine quinone]]
[[Category: trihydroxyphenylalanine quinone]]


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