1rjo

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(New page: 200px<br /><applet load="1rjo" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rjo, resolution 1.67&Aring;" /> '''AGAO + Xe'''<br /> ...)
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[[Image:1rjo.gif|left|200px]]<br /><applet load="1rjo" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1rjo.gif|left|200px]]<br /><applet load="1rjo" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1rjo, resolution 1.67&Aring;" />
caption="1rjo, resolution 1.67&Aring;" />
'''AGAO + Xe'''<br />
'''AGAO + Xe'''<br />
==Overview==
==Overview==
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Potential dioxygen-binding sites in three Cu amine oxidases have been, investigated by recording X-ray diffraction data at 1.7-2.2A resolution, for crystals under a high pressure of xenon gas. Electron-density, difference maps and crystallographic refinement provide unequivocal, evidence for a number of Xe-binding sites in each enzyme. Only one of, these sites is present in all three Cu amine oxidases studied. Structural, changes elsewhere in the protein molecules are insignificant. The results, illustrate the use of xenon as a probe for cavities, in which a protein, may accommodate a dioxygen molecule. The finding of a potential, dioxygen-binding cavity close to the active site of Cu amine oxidases may, be relevant to the function of the enzymes, since the formation of a, transient protein-dioxygen complex is a likely step in the catalytic, mechanism. No evidence was found for xenon binding in a region of the, molecule that was previously identified in two other Cu amine oxidases as, a potential transient dioxygen-binding site.
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Potential dioxygen-binding sites in three Cu amine oxidases have been investigated by recording X-ray diffraction data at 1.7-2.2A resolution for crystals under a high pressure of xenon gas. Electron-density difference maps and crystallographic refinement provide unequivocal evidence for a number of Xe-binding sites in each enzyme. Only one of these sites is present in all three Cu amine oxidases studied. Structural changes elsewhere in the protein molecules are insignificant. The results illustrate the use of xenon as a probe for cavities, in which a protein may accommodate a dioxygen molecule. The finding of a potential dioxygen-binding cavity close to the active site of Cu amine oxidases may be relevant to the function of the enzymes, since the formation of a transient protein-dioxygen complex is a likely step in the catalytic mechanism. No evidence was found for xenon binding in a region of the molecule that was previously identified in two other Cu amine oxidases as a potential transient dioxygen-binding site.
==About this Structure==
==About this Structure==
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1RJO 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, XE 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=1RJO OCA].
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1RJO 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>, <scene name='pdbligand=XE:'>XE</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=1RJO OCA].
==Reference==
==Reference==
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[[Category: Arthrobacter globiformis]]
[[Category: Arthrobacter globiformis]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Duff, A.P.]]
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[[Category: Duff, A P.]]
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[[Category: Guss, J.M.]]
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[[Category: Guss, J M.]]
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[[Category: Trambaiolo, D.M.]]
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[[Category: Trambaiolo, D M.]]
[[Category: CU]]
[[Category: CU]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: xenon]]
[[Category: xenon]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 01:39:03 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:51:34 2008''

Revision as of 12:51, 21 February 2008


1rjo, resolution 1.67Å

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AGAO + Xe

Overview

Potential dioxygen-binding sites in three Cu amine oxidases have been investigated by recording X-ray diffraction data at 1.7-2.2A resolution for crystals under a high pressure of xenon gas. Electron-density difference maps and crystallographic refinement provide unequivocal evidence for a number of Xe-binding sites in each enzyme. Only one of these sites is present in all three Cu amine oxidases studied. Structural changes elsewhere in the protein molecules are insignificant. The results illustrate the use of xenon as a probe for cavities, in which a protein may accommodate a dioxygen molecule. The finding of a potential dioxygen-binding cavity close to the active site of Cu amine oxidases may be relevant to the function of the enzymes, since the formation of a transient protein-dioxygen complex is a likely step in the catalytic mechanism. No evidence was found for xenon binding in a region of the molecule that was previously identified in two other Cu amine oxidases as a potential transient dioxygen-binding site.

About this Structure

1RJO is a Single protein structure of sequence from Arthrobacter globiformis with , , , and as ligands. Active as Amine oxidase (copper-containing), with EC number 1.4.3.6 Full crystallographic information is available from OCA.

Reference

Using xenon as a probe for dioxygen-binding sites in copper amine oxidases., Duff AP, Trambaiolo DM, Cohen AE, Ellis PJ, Juda GA, Shepard EM, Langley DB, Dooley DM, Freeman HC, Guss JM, J Mol Biol. 2004 Nov 26;344(3):599-607. PMID:15533431

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