1hy3: Difference between revisions

New page: left|200px<br /> <applet load="1hy3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1hy3, resolution 1.80Å" /> '''CRYSTAL STRUCTURE O...
 
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[[Image:1hy3.gif|left|200px]]<br />
[[Image:1hy3.gif|left|200px]]<br /><applet load="1hy3" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1hy3" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1hy3, resolution 1.80&Aring;" />
caption="1hy3, resolution 1.80&Aring;" />
'''CRYSTAL STRUCTURE OF HUMAN ESTROGEN SULFOTRANSFERASE V269E MUTANT IN THE PRESENCE OF PAPS'''<br />
'''CRYSTAL STRUCTURE OF HUMAN ESTROGEN SULFOTRANSFERASE V269E MUTANT IN THE PRESENCE OF PAPS'''<br />


==Overview==
==Overview==
Estrogen sulfotransferase (EST) transfers the sulfate group from, 3'-phosphoadenosine 5'-phosphosulfate (PAPS) to estrogenic steroids. Here, we report the crystal structure of human EST (hEST) in the context of the, V269E mutant-PAPS complex, which is the first structure containing the, active sulfate donor for any sulfotransferase. Superimposing this, structure with the crystal structure of hEST in complex with the donor, product 3'-phosphoadenosine 5'-phosphate (PAP) and the acceptor substrate, 17beta-estradiol, the ternary structure with the PAPS and estradiol, molecule, is modeled. These structures have now provided a more complete, view of the S(N)2-like in-line displacement reaction catalyzed by, sulfotransferases. In the PAPS-bound structure, the side chain nitrogen of, the catalytic Lys(47) interacts with the side chain hydroxyl of Ser(137), and not with the bridging oxygen between the 5'-phosphate and sulfate, groups of the PAPS molecule as is seen in the PAP-bound structures. This, conformational change of the side chain nitrogen indicates that the, interaction of Lys(47) with Ser(137) may regulate PAPS hydrolysis in the, absences of an acceptor substrate. Supporting the structural data, the, mutations of Ser(137) to cysteine and alanine decrease gradually k(cat), for PAPS hydrolysis and transfer activity. Thus, Ser(137) appears to play, an important role in regulating the side chain interaction of Lys(47) with, the bridging oxygen between the 5'-phosphate and the sulfate of PAPS.
Estrogen sulfotransferase (EST) transfers the sulfate group from 3'-phosphoadenosine 5'-phosphosulfate (PAPS) to estrogenic steroids. Here we report the crystal structure of human EST (hEST) in the context of the V269E mutant-PAPS complex, which is the first structure containing the active sulfate donor for any sulfotransferase. Superimposing this structure with the crystal structure of hEST in complex with the donor product 3'-phosphoadenosine 5'-phosphate (PAP) and the acceptor substrate 17beta-estradiol, the ternary structure with the PAPS and estradiol molecule, is modeled. These structures have now provided a more complete view of the S(N)2-like in-line displacement reaction catalyzed by sulfotransferases. In the PAPS-bound structure, the side chain nitrogen of the catalytic Lys(47) interacts with the side chain hydroxyl of Ser(137) and not with the bridging oxygen between the 5'-phosphate and sulfate groups of the PAPS molecule as is seen in the PAP-bound structures. This conformational change of the side chain nitrogen indicates that the interaction of Lys(47) with Ser(137) may regulate PAPS hydrolysis in the absences of an acceptor substrate. Supporting the structural data, the mutations of Ser(137) to cysteine and alanine decrease gradually k(cat) for PAPS hydrolysis and transfer activity. Thus, Ser(137) appears to play an important role in regulating the side chain interaction of Lys(47) with the bridging oxygen between the 5'-phosphate and the sulfate of PAPS.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1HY3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with PPS as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Estrone_sulfotransferase Estrone sulfotransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.8.2.4 2.8.2.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1HY3 OCA].  
1HY3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=PPS:'>PPS</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Estrone_sulfotransferase Estrone sulfotransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.8.2.4 2.8.2.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HY3 OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Negishi, M.]]
[[Category: Negishi, M.]]
[[Category: Pedersen, L.C.]]
[[Category: Pedersen, L C.]]
[[Category: Petrochenko, E.V.]]
[[Category: Petrochenko, E V.]]
[[Category: Shevtsov, S.]]
[[Category: Shevtsov, S.]]
[[Category: PPS]]
[[Category: PPS]]
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[[Category: sulfotransferase]]
[[Category: sulfotransferase]]


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