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 | 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 >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:// | 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 | [[Category: Markley, J L.]] | ||
[[Category: Morgan, C | [[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]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:30:13 2008'' |