8rij

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Current revision (07:06, 3 July 2025) (edit) (undo)
 
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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=8rij FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8rij OCA], [https://pdbe.org/8rij PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8rij RCSB], [https://www.ebi.ac.uk/pdbsum/8rij PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8rij ProSAT]</span></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=8rij FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8rij OCA], [https://pdbe.org/8rij PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8rij RCSB], [https://www.ebi.ac.uk/pdbsum/8rij PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8rij ProSAT]</span></td></tr>
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== Function ==
 
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[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.
 
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Current revision

Discovery of the first orally bioavailable ADAMTS7 inhibitor BAY-9835

PDB ID 8rij

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