4gr3: Difference between revisions
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== | ==Crystal structure of the catalytic domain of Human MMP12 in complex with selective phosphinic inhibitor RXP470A== | ||
[[http://www.uniprot.org/uniprot/MMP12_HUMAN MMP12_HUMAN | <StructureSection load='4gr3' size='340' side='right'caption='[[4gr3]], [[Resolution|resolution]] 1.49Å' scene=''> | ||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[4gr3]] is a 1 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=4GR3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4GR3 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.494Å</td></tr> | |||
<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=R45:N-{(2S)-3-[(S)-(4-BROMOPHENYL)(HYDROXY)PHOSPHORYL]-2-[(3-PHENYL-1,2-OXAZOL-5-YL)METHYL]PROPANOYL}-L-ALPHA-GLUTAMYL-L-ALPHA-GLUTAMINE'>R45</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4gr3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gr3 OCA], [https://pdbe.org/4gr3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4gr3 RCSB], [https://www.ebi.ac.uk/pdbsum/4gr3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4gr3 ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/MMP12_HUMAN MMP12_HUMAN] May be involved in tissue injury and remodeling. Has significant elastolytic activity. Can accept large and small amino acids at the P1' site, but has a preference for leucine. Aromatic or hydrophobic residues are preferred at the P1 site, with small hydrophobic residues (preferably alanine) occupying P3. | |||
== | ==See Also== | ||
[[ | *[[Matrix metalloproteinase 3D structures|Matrix metalloproteinase 3D structures]] | ||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: Beau | [[Category: Beau F]] | ||
[[Category: Cassar-Lajeunesse | [[Category: Cassar-Lajeunesse E]] | ||
[[Category: Devel | [[Category: Devel L]] | ||
[[Category: Dive | [[Category: Dive V]] | ||
[[Category: Stura | [[Category: Stura EA]] | ||
[[Category: Vera | [[Category: Vera L]] | ||
Latest revision as of 15:53, 14 March 2024
Crystal structure of the catalytic domain of Human MMP12 in complex with selective phosphinic inhibitor RXP470A
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