2arf: Difference between revisions

New page: left|200px<br /> <applet load="2arf" size="450" color="white" frame="true" align="right" spinBox="true" caption="2arf" /> '''Solution structure of the Wilson ATPase N-d...
 
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'''Solution structure of the Wilson ATPase N-domain in the presence of ATP'''<br />
'''Solution structure of the Wilson ATPase N-domain in the presence of ATP'''<br />


==Overview==
==Overview==
Wilson disease protein (ATP7B) is a copper-transporting P(1B)-type ATPase, that regulates copper homeostasis and biosynthesis of copper-containing, enzymes in human tissues. Inactivation of ATP7B or related ATP7A leads to, severe neurodegenerative disorders, whereas their overexpression, contributes to cancer cell resistance to chemotherapeutics., Copper-transporting ATPases differ from other P-type ATPases in their, topology and the sequence of their nucleotide-binding domain (N-domain)., To gain insight into the structural basis of ATP7B function, we have, solved the structure of the ATP7B N-domain in the presence of ATP by using, heteronuclear multidimensional NMR spectroscopy. The N-domain consists of, a six-stranded beta-sheet with two adjacent alpha-helical hairpins and, unexpectedly, shows higher similarity to the bacterial K(+)-transporting, ATPase KdpB than to the mammalian Ca(2+)-ATPase or Na(+),K(+)-ATPase. The, common core structure of P-type ATPases is retained in the 3D fold of the, N-domain; however, the nucleotide coordination environment of ATP7B within, this fold is different. The residues H1069, G1099, G1101, I1102, G1149, and N1150 conserved in the P(1B)-ATPase subfamily contribute to ATP, binding. Analysis of the frequent disease mutation H1069Q demonstrates, that this mutation does not significantly affect the structure of the, N-domain but prevents tight binding of ATP. The structure of the N-domain, accounts for the disruptive effects of &gt;30 known Wilson disease mutations., The unique features of the N-domain provide a structural basis for the, development of specific inhibitors and regulators of ATP7B.
Wilson disease protein (ATP7B) is a copper-transporting P(1B)-type ATPase that regulates copper homeostasis and biosynthesis of copper-containing enzymes in human tissues. Inactivation of ATP7B or related ATP7A leads to severe neurodegenerative disorders, whereas their overexpression contributes to cancer cell resistance to chemotherapeutics. Copper-transporting ATPases differ from other P-type ATPases in their topology and the sequence of their nucleotide-binding domain (N-domain). To gain insight into the structural basis of ATP7B function, we have solved the structure of the ATP7B N-domain in the presence of ATP by using heteronuclear multidimensional NMR spectroscopy. The N-domain consists of a six-stranded beta-sheet with two adjacent alpha-helical hairpins and, unexpectedly, shows higher similarity to the bacterial K(+)-transporting ATPase KdpB than to the mammalian Ca(2+)-ATPase or Na(+),K(+)-ATPase. The common core structure of P-type ATPases is retained in the 3D fold of the N-domain; however, the nucleotide coordination environment of ATP7B within this fold is different. The residues H1069, G1099, G1101, I1102, G1149, and N1150 conserved in the P(1B)-ATPase subfamily contribute to ATP binding. Analysis of the frequent disease mutation H1069Q demonstrates that this mutation does not significantly affect the structure of the N-domain but prevents tight binding of ATP. The structure of the N-domain accounts for the disruptive effects of &gt;30 known Wilson disease mutations. The unique features of the N-domain provide a structural basis for the development of specific inhibitors and regulators of ATP7B.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
2ARF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Copper-exporting_ATPase Copper-exporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.4 3.6.3.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2ARF OCA].  
2ARF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Copper-exporting_ATPase Copper-exporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.4 3.6.3.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ARF OCA].  


==Reference==
==Reference==
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[[Category: Dmitriev, O.]]
[[Category: Dmitriev, O.]]
[[Category: Lutsenko, S.]]
[[Category: Lutsenko, S.]]
[[Category: Markley, J.L.]]
[[Category: Markley, J L.]]
[[Category: Morgan, C.T.]]
[[Category: Morgan, C T.]]
[[Category: Tsivkovskii, R.]]
[[Category: Tsivkovskii, R.]]
[[Category: atp binding]]
[[Category: atp binding]]
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[[Category: wilson disease]]
[[Category: wilson disease]]


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