9hz0: Difference between revisions

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New page: '''Unreleased structure''' The entry 9hz0 is ON HOLD Authors: Wiese, J.N., Mueller, M.P., Rauh, D. Description: Protein kinase MKK7 in complex with K221 targeting compound 1 [[Category...
 
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'''Unreleased structure'''


The entry 9hz0 is ON HOLD
==Protein kinase MKK7 in complex with K221 targeting compound 1==
 
<StructureSection load='9hz0' size='340' side='right'caption='[[9hz0]], [[Resolution|resolution]] 2.25&Aring;' scene=''>
Authors: Wiese, J.N., Mueller, M.P., Rauh, D.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9hz0]] 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=9HZ0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9HZ0 FirstGlance]. <br>
Description: Protein kinase MKK7 in complex with K221 targeting compound 1
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.25&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1IY7:5-(2~{H}-indazol-3-yl)-2-methyl-phenol'>A1IY7</scene></td></tr>
[[Category: Mueller, M.P]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9hz0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9hz0 OCA], [https://pdbe.org/9hz0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9hz0 RCSB], [https://www.ebi.ac.uk/pdbsum/9hz0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9hz0 ProSAT]</span></td></tr>
[[Category: Wiese, J.N]]
</table>
[[Category: Rauh, D]]
== Function ==
[https://www.uniprot.org/uniprot/MP2K7_HUMAN MP2K7_HUMAN] Dual specificity protein kinase which acts as an essential component of the MAP kinase signal transduction pathway. Essential component of the stress-activated protein kinase/c-Jun N-terminal kinase (SAP/JNK) signaling pathway. With MAP2K4/MKK4, is the one of the only known kinase to directly activate the stress-activated protein kinase/c-Jun N-terminal kinases MAPK8/JNK1, MAPK9/JNK2 and MAPK10/JNK3. MAP2K4/MKK4 and MAP2K7/MKK7 both activate the JNKs by phosphorylation, but they differ in their preference for the phosphorylation site in the Thr-Pro-Tyr motif. MAP2K4/MKK4 shows preference for phosphorylation of the Tyr residue and MAP2K7/MKK7 for the Thr residue. The monophosphorylation of JNKs on the Thr residue is sufficient to increase JNK activity indicating that MAP2K7/MKK7 is important to trigger JNK activity, while the additional phosphorylation of the Tyr residue by MAP2K4/MKK4 ensures optimal JNK activation. Has a specific role in JNK signal transduction pathway activated by proinflammatory cytokines. The MKK/JNK signaling pathway is also involved in mitochondrial death signaling pathway, including the release cytochrome c, leading to apoptosis.<ref>PMID:9372971</ref> <ref>PMID:9312068</ref> <ref>PMID:9535930</ref> [:]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Mueller MP]]
[[Category: Rauh D]]
[[Category: Wiese JN]]

Latest revision as of 08:30, 4 June 2025

Protein kinase MKK7 in complex with K221 targeting compound 1

9hz0, resolution 2.25Å

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