1zp5

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(New page: 200px<br /> <applet load="1zp5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1zp5, resolution 1.80&Aring;" /> '''Crystal structure o...)
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<applet load="1zp5" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1zp5, resolution 1.80&Aring;" />
'''Crystal structure of the complex between MMP-8 and a N-hydroxyurea inhibitor'''<br />
'''Crystal structure of the complex between MMP-8 and a N-hydroxyurea inhibitor'''<br />
==Overview==
==Overview==
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The first crystallographic structure of an N-hydroxyurea inhibitor bound, into the active site of a matrix metalloproteinase is reported. The ligand, and three other analogues were prepared and studied as inhibitors of, MMP-2, MMP-3, and MMP-8. The crystal structure of the complex with MMP-8, shows that the N-hydroxyurea, contrary to the analogous hydroxamate, binds, the catalytic zinc ion in a monodentate rather than bidentate mode and, with high out-of-plane distortion of the amide bonds.
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The first crystallographic structure of an N-hydroxyurea inhibitor bound into the active site of a matrix metalloproteinase is reported. The ligand and three other analogues were prepared and studied as inhibitors of MMP-2, MMP-3, and MMP-8. The crystal structure of the complex with MMP-8 shows that the N-hydroxyurea, contrary to the analogous hydroxamate, binds the catalytic zinc ion in a monodentate rather than bidentate mode and with high out-of-plane distortion of the amide bonds.
==About this Structure==
==About this Structure==
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1ZP5 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 CA, ZN and 2NI as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Neutrophil_collagenase Neutrophil collagenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.34 3.4.24.34] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ZP5 OCA].
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1ZP5 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=CA:'>CA</scene>, <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=2NI:'>2NI</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Neutrophil_collagenase Neutrophil collagenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.34 3.4.24.34] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZP5 OCA].
==Reference==
==Reference==
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[[Category: hydrolase]]
[[Category: hydrolase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:38:09 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:17:50 2008''

Revision as of 14:17, 21 February 2008


1zp5, resolution 1.80Å

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Crystal structure of the complex between MMP-8 and a N-hydroxyurea inhibitor

Overview

The first crystallographic structure of an N-hydroxyurea inhibitor bound into the active site of a matrix metalloproteinase is reported. The ligand and three other analogues were prepared and studied as inhibitors of MMP-2, MMP-3, and MMP-8. The crystal structure of the complex with MMP-8 shows that the N-hydroxyurea, contrary to the analogous hydroxamate, binds the catalytic zinc ion in a monodentate rather than bidentate mode and with high out-of-plane distortion of the amide bonds.

About this Structure

1ZP5 is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as Neutrophil collagenase, with EC number 3.4.24.34 Full crystallographic information is available from OCA.

Reference

N-Hydroxyurea as zinc binding group in matrix metalloproteinase inhibition: mode of binding in a complex with MMP-8., Campestre C, Agamennone M, Tortorella P, Preziuso S, Biasone A, Gavuzzo E, Pochetti G, Mazza F, Hiller O, Tschesche H, Consalvi V, Gallina C, Bioorg Med Chem Lett. 2006 Jan 1;16(1):20-4. Epub 2005 Oct 18. PMID:16242329

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