966c

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(New page: 200px<br /> <applet load="966c" size="450" color="white" frame="true" align="right" spinBox="true" caption="966c, resolution 1.9&Aring;" /> '''CRYSTAL STRUCTURE OF...)
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[[Image:966c.gif|left|200px]]<br /><applet load="966c" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="966c" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="966c, resolution 1.9&Aring;" />
caption="966c, resolution 1.9&Aring;" />
'''CRYSTAL STRUCTURE OF FIBROBLAST COLLAGENASE-1 COMPLEXED TO A DIPHENYL-ETHER SULPHONE BASED HYDROXAMIC ACID'''<br />
'''CRYSTAL STRUCTURE OF FIBROBLAST COLLAGENASE-1 COMPLEXED TO A DIPHENYL-ETHER SULPHONE BASED HYDROXAMIC ACID'''<br />
==Overview==
==Overview==
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The X-ray crystal structures of the catalytic domain of human, collagenase-3 (MMP-13) and collagenase-1 (MMP-1) with bound inhibitors, provides a basis for understanding the selectivity profile of a novel, series of matrix metalloprotease (MMP) inhibitors. Differences in the, relative size and shape of the MMP S1' pockets suggest that this pocket is, a critical determinant of MMP inhibitor selectivity. The collagenase-3 S1', pocket is long and open, easily accommodating large P1' groups, such as, diphenylether. In contrast, the collagenase-1 S1' pocket must undergo a, conformational change to accommodate comparable P1' groups. The, selectivity of the diphenylether series of inhibitors for collagenase-3 is, largely determined by their affinity for the preformed S1' pocket of, collagenase-3, as compared to the induced fit in collagenase-1.
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The X-ray crystal structures of the catalytic domain of human collagenase-3 (MMP-13) and collagenase-1 (MMP-1) with bound inhibitors provides a basis for understanding the selectivity profile of a novel series of matrix metalloprotease (MMP) inhibitors. Differences in the relative size and shape of the MMP S1' pockets suggest that this pocket is a critical determinant of MMP inhibitor selectivity. The collagenase-3 S1' pocket is long and open, easily accommodating large P1' groups, such as diphenylether. In contrast, the collagenase-1 S1' pocket must undergo a conformational change to accommodate comparable P1' groups. The selectivity of the diphenylether series of inhibitors for collagenase-3 is largely determined by their affinity for the preformed S1' pocket of collagenase-3, as compared to the induced fit in collagenase-1.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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966C 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 ZN, CA and RS2 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=966C OCA].
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966C 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=ZN:'>ZN</scene>, <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=RS2:'>RS2</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=966C OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Broka, C.]]
[[Category: Broka, C.]]
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[[Category: Browner, M.F.]]
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[[Category: Browner, M F.]]
[[Category: Campbell, J.]]
[[Category: Campbell, J.]]
[[Category: Carr, S.]]
[[Category: Carr, S.]]
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[[Category: Hendricks, R.T.]]
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[[Category: Hendricks, R T.]]
[[Category: Lovejoy, B.]]
[[Category: Lovejoy, B.]]
[[Category: Luong, C.]]
[[Category: Luong, C.]]
[[Category: Martin, R.]]
[[Category: Martin, R.]]
[[Category: Walker, K.]]
[[Category: Walker, K.]]
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[[Category: Wart, H.Van.]]
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[[Category: Wart, H Van.]]
[[Category: Welch, A.]]
[[Category: Welch, A.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: matrix metalloprotease]]
[[Category: matrix metalloprotease]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 23:56:02 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:18:22 2008''

Revision as of 17:18, 21 February 2008


966c, resolution 1.9Å

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CRYSTAL STRUCTURE OF FIBROBLAST COLLAGENASE-1 COMPLEXED TO A DIPHENYL-ETHER SULPHONE BASED HYDROXAMIC ACID

Contents

Overview

The X-ray crystal structures of the catalytic domain of human collagenase-3 (MMP-13) and collagenase-1 (MMP-1) with bound inhibitors provides a basis for understanding the selectivity profile of a novel series of matrix metalloprotease (MMP) inhibitors. Differences in the relative size and shape of the MMP S1' pockets suggest that this pocket is a critical determinant of MMP inhibitor selectivity. The collagenase-3 S1' pocket is long and open, easily accommodating large P1' groups, such as diphenylether. In contrast, the collagenase-1 S1' pocket must undergo a conformational change to accommodate comparable P1' groups. The selectivity of the diphenylether series of inhibitors for collagenase-3 is largely determined by their affinity for the preformed S1' pocket of collagenase-3, as compared to the induced fit in collagenase-1.

Disease

Known diseases associated with this structure: COPD, rate of decline of lung function in OMIM:[120353]

About this Structure

966C is a Single protein structure of sequence from Homo sapiens with , and as ligands. Full crystallographic information is available from OCA.

Reference

Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors., Lovejoy B, Welch AR, Carr S, Luong C, Broka C, Hendricks RT, Campbell JA, Walker KA, Martin R, Van Wart H, Browner MF, Nat Struct Biol. 1999 Mar;6(3):217-21. PMID:10074939

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