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New page: left|200px<br /> <applet load="4ayk" size="450" color="white" frame="true" align="right" spinBox="true" caption="4ayk" /> '''CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLL...
 
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[[Image:4ayk.gif|left|200px]]<br />
[[Image:4ayk.gif|left|200px]]<br /><applet load="4ayk" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="4ayk" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="4ayk" />
caption="4ayk" />
'''CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE COMPLEXED WITH CGS-27023A, NMR, 30 STRUCTURES'''<br />
'''CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE COMPLEXED WITH CGS-27023A, NMR, 30 STRUCTURES'''<br />


==Overview==
==Overview==
The solution structure of the catalytic fragment of human fibroblast, collagenase (MMP-1) complexed with a sulfonamide derivative of a, hydroxamic acid compound (CGS-27023A) has been determined using, two-dimensional and three-dimensional heteronuclear NMR spectroscopy. The, solution structure of the complex was calculated by means of hybrid, distance geometry-simulated annealing using a combination of experimental, NMR restraints obtained from the previous refinement of the inhibitor-free, MMP-1 (1) and recent restraints for the MMP-1:CGS-27023A complex. The, hydroxamic acid moiety of CGS-27023A was found to chelate to the "right", of the catalytic zinc where the p-methoxyphenyl sits in the S1', active-site pocket, the isopropyl group is in contact with H83 and N80, and the pyridine ring is solvent exposed. The sulfonyl oxygens are in, hydrogen-bonding distance to the backbone NHs of L81 and A82. This is, similar to the conformation determined by NMR of the inhibitor bound to, stromelysin (2, 3). A total of 48 distance restraints were observed, between MMP-1 and CGS-27023A from 3D 13C-edited/12C-filtered NOESY and 3D, 15N-edited NOESY experiments. An additional 18 intramolecular restraints, were observed for CGS-27023A from a 2D 12C-filtered NOESY experiment. A, minimal set of NMR experiments in combination with the free MMP-1, assignments were used to assign the MMP-1 (1)H, 13C, and 15N resonances in, the MMP-1:CGS-27023A complex. The assignments of CGS-27023A in the complex, were obtained from 2D 12C-filtered NOESY and 2D 12C-filtered TOCSY, experiments.
The solution structure of the catalytic fragment of human fibroblast collagenase (MMP-1) complexed with a sulfonamide derivative of a hydroxamic acid compound (CGS-27023A) has been determined using two-dimensional and three-dimensional heteronuclear NMR spectroscopy. The solution structure of the complex was calculated by means of hybrid distance geometry-simulated annealing using a combination of experimental NMR restraints obtained from the previous refinement of the inhibitor-free MMP-1 (1) and recent restraints for the MMP-1:CGS-27023A complex. The hydroxamic acid moiety of CGS-27023A was found to chelate to the "right" of the catalytic zinc where the p-methoxyphenyl sits in the S1' active-site pocket, the isopropyl group is in contact with H83 and N80, and the pyridine ring is solvent exposed. The sulfonyl oxygens are in hydrogen-bonding distance to the backbone NHs of L81 and A82. This is similar to the conformation determined by NMR of the inhibitor bound to stromelysin (2, 3). A total of 48 distance restraints were observed between MMP-1 and CGS-27023A from 3D 13C-edited/12C-filtered NOESY and 3D 15N-edited NOESY experiments. An additional 18 intramolecular restraints were observed for CGS-27023A from a 2D 12C-filtered NOESY experiment. A minimal set of NMR experiments in combination with the free MMP-1 assignments were used to assign the MMP-1 (1)H, 13C, and 15N resonances in the MMP-1:CGS-27023A complex. The assignments of CGS-27023A in the complex were obtained from 2D 12C-filtered NOESY and 2D 12C-filtered TOCSY experiments.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
4AYK 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 CGS as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Interstitial_collagenase Interstitial collagenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.7 3.4.24.7] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=4AYK OCA].  
4AYK 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=CGS:'>CGS</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Interstitial_collagenase Interstitial collagenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.7 3.4.24.7] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AYK OCA].  


==Reference==
==Reference==
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[[Category: Interstitial collagenase]]
[[Category: Interstitial collagenase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Moy, F.J.]]
[[Category: Moy, F J.]]
[[Category: Powers, R.]]
[[Category: Powers, R.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: metalloprotease]]
[[Category: metalloprotease]]


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