1hy7

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{{STRUCTURE_1hy7| PDB=1hy7 | SCENE= }}
 
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===A CARBOXYLIC ACID BASED INHIBITOR IN COMPLEX WITH MMP3===
 
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{{ABSTRACT_PUBMED_11297453}}
 
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==Disease==
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==A CARBOXYLIC ACID BASED INHIBITOR IN COMPLEX WITH MMP3==
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[[http://www.uniprot.org/uniprot/MMP3_HUMAN MMP3_HUMAN]] Defects in MMP3 are the cause of susceptibility to coronary heart disease type 6 (CHDS6) [MIM:[http://omim.org/entry/614466 614466]]. A multifactorial disease characterized by an imbalance between myocardial functional requirements and the capacity of the coronary vessels to supply sufficient blood flow. Decreased capacity of the coronary vessels is often associated with thickening and loss of elasticity of the coronary arteries. Note=A polymorphism in the MMP3 promoter region is associated with the risk of coronary heart disease and myocardial infarction, due to lower MMP3 proteolytic activity and higher extracellular matrix deposition in atherosclerotic lesions.<ref>PMID:8662692</ref><ref>PMID:12477941</ref>
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<StructureSection load='1hy7' size='340' side='right'caption='[[1hy7]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
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== Structural highlights ==
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==Function==
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<table><tr><td colspan='2'>[[1hy7]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HY7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1HY7 FirstGlance]. <br>
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[[http://www.uniprot.org/uniprot/MMP3_HUMAN MMP3_HUMAN]] Can degrade fibronectin, laminin, gelatins of type I, III, IV, and V; collagens III, IV, X, and IX, and cartilage proteoglycans. Activates procollagenase.
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.5&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=MBS:R-2-{[4-METHOXY-(1,1-BIPHENYL)-4-YL]-SULFONYL}-AMINO-6-METHOXY-HEX-4-YNOIC+ACID'>MBS</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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==About this Structure==
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1hy7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1hy7 OCA], [https://pdbe.org/1hy7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1hy7 RCSB], [https://www.ebi.ac.uk/pdbsum/1hy7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1hy7 ProSAT]</span></td></tr>
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[[1hy7]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HY7 OCA].
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/MMP3_HUMAN MMP3_HUMAN] Defects in MMP3 are the cause of susceptibility to coronary heart disease type 6 (CHDS6) [MIM:[https://omim.org/entry/614466 614466]. A multifactorial disease characterized by an imbalance between myocardial functional requirements and the capacity of the coronary vessels to supply sufficient blood flow. Decreased capacity of the coronary vessels is often associated with thickening and loss of elasticity of the coronary arteries. Note=A polymorphism in the MMP3 promoter region is associated with the risk of coronary heart disease and myocardial infarction, due to lower MMP3 proteolytic activity and higher extracellular matrix deposition in atherosclerotic lesions.<ref>PMID:8662692</ref> <ref>PMID:12477941</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/MMP3_HUMAN MMP3_HUMAN] Can degrade fibronectin, laminin, gelatins of type I, III, IV, and V; collagens III, IV, X, and IX, and cartilage proteoglycans. Activates procollagenase.
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/hy/1hy7_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1hy7 ConSurf].
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<div style="clear:both"></div>
==See Also==
==See Also==
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*[[Matrix metalloproteinase|Matrix metalloproteinase]]
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*[[Matrix metalloproteinase 3D structures|Matrix metalloproteinase 3D structures]]
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== References ==
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==Reference==
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<references/>
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<ref group="xtra">PMID:011297453</ref><references group="xtra"/><references/>
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__TOC__
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Stromelysin 1]]
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[[Category: Large Structures]]
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[[Category: Almstead, N G.]]
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[[Category: Almstead NG]]
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[[Category: Baker, T R.]]
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[[Category: Baker TR]]
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[[Category: Bookland, R G.]]
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[[Category: Bookland RG]]
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[[Category: Branch, T M.]]
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[[Category: Branch TM]]
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[[Category: De, B.]]
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[[Category: De B]]
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[[Category: Foltz, D J.]]
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[[Category: Foltz DJ]]
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[[Category: Garver, S M.]]
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[[Category: Garver SM]]
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[[Category: Gu, F.]]
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[[Category: Gu F]]
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[[Category: Hsieh, L C.]]
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[[Category: Hsieh LC]]
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[[Category: Janusz, M J.]]
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[[Category: Janusz MJ]]
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[[Category: King, S L.]]
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[[Category: King SL]]
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[[Category: Laufersweiler, M J.]]
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[[Category: Laufersweiler MJ]]
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[[Category: Mieling, G E.]]
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[[Category: Mieling GE]]
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[[Category: Natchus, M G.]]
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[[Category: Natchus MG]]
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[[Category: Patel, V S.]]
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[[Category: Patel VS]]
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[[Category: Peng, S X.]]
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[[Category: Peng SX]]
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[[Category: Pikul, S.]]
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[[Category: Pikul S]]
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[[Category: Pokross, M E.]]
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[[Category: Pokross ME]]
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[[Category: Hydrolase]]
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[[Category: Inhibited]]
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[[Category: Mixed alpha beta structure]]
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[[Category: Zinc protease]]
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Current revision

A CARBOXYLIC ACID BASED INHIBITOR IN COMPLEX WITH MMP3

PDB ID 1hy7

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Proteopedia Page Contributors and Editors (what is this?)

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