5v19

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'''Unreleased structure'''
 
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The entry 5v19 is ON HOLD
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==Structure-based drug design of novel ASK1 inhibitors using a fully integrated lead optimization strategy==
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<StructureSection load='5v19' size='340' side='right'caption='[[5v19]], [[Resolution|resolution]] 3.10&Aring;' scene=''>
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Authors: Dougan, D.R., Lawson, J.D., Lane, W.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5v19]] 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=5V19 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5V19 FirstGlance]. <br>
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Description: Structure-based drug design of novel ASK1 inhibitors using a fully integrated lead optimization strategy
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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]] 3.1&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=8V4:N-(1-ETHYL-1H-PYRAZOL-4-YL)FURAN-3-CARBOXAMIDE'>8V4</scene></td></tr>
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[[Category: Lawson, J.D]]
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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=5v19 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5v19 OCA], [https://pdbe.org/5v19 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5v19 RCSB], [https://www.ebi.ac.uk/pdbsum/5v19 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5v19 ProSAT]</span></td></tr>
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[[Category: Dougan, D.R]]
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</table>
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[[Category: Lane, W]]
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== Function ==
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[https://www.uniprot.org/uniprot/M3K5_HUMAN M3K5_HUMAN] Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway. Plays an important role in the cascades of cellular responses evoked by changes in the environment. Mediates signaling for determination of cell fate such as differentiation and survival. Plays a crucial role in the apoptosis signal transduction pathway through mitochondria-dependent caspase activation. MAP3K5/ASK1 is required for the innate immune response, which is essential for host defense against a wide range of pathogens. Mediates signal transduction of various stressors like oxidative stress as well as by receptor-mediated inflammatory signals, such as the tumor necrosis factor (TNF) or lipopolysaccharide (LPS). Once activated, acts as an upstream activator of the MKK/JNK signal transduction cascade and the p38 MAPK signal transduction cascade through the phosphorylation and activation of several MAP kinase kinases like MAP2K4/SEK1, MAP2K3/MKK3, MAP2K6/MKK6 and MAP2K7/MKK7. These MAP2Ks in turn activate p38 MAPKs and c-jun N-terminal kinases (JNKs). Both p38 MAPK and JNKs control the transcription factors activator protein-1 (AP-1).<ref>PMID:8940179</ref> <ref>PMID:8974401</ref> <ref>PMID:9564042</ref> <ref>PMID:9774977</ref> <ref>PMID:10411906</ref> <ref>PMID:10849426</ref> <ref>PMID:10688666</ref> <ref>PMID:11689443</ref> <ref>PMID:11029458</ref> <ref>PMID:11154276</ref> <ref>PMID:14749717</ref> <ref>PMID:11920685</ref> <ref>PMID:12697749</ref> <ref>PMID:15023544</ref> <ref>PMID:14688258</ref> <ref>PMID:16129676</ref> <ref>PMID:17220297</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Dougan DR]]
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[[Category: Lane W]]
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[[Category: Lawson JD]]

Current revision

Structure-based drug design of novel ASK1 inhibitors using a fully integrated lead optimization strategy

PDB ID 5v19

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