|  |   | 
		| Line 1: | Line 1: | 
|  |  |  |  | 
|  | ==A kinase complex MST4-MOB4== |  | ==A kinase complex MST4-MOB4== | 
| - | <StructureSection load='5yf4' size='340' side='right' caption='[[5yf4]], [[Resolution|resolution]] 1.90Å' scene=''> | + | <StructureSection load='5yf4' size='340' side='right'caption='[[5yf4]], [[Resolution|resolution]] 1.90Å' scene=''> | 
|  | == Structural highlights == |  | == Structural highlights == | 
| - | <table><tr><td colspan='2'>[[5yf4]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5YF4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5YF4 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[5yf4]] 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=5YF4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5YF4 FirstGlance]. <br> | 
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.897Å</td></tr> | 
| - | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | 
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">MOB4,MOB3, MOBKL3, PHOCN, PREI3, CGI-95 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=5yf4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5yf4 OCA], [https://pdbe.org/5yf4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5yf4 RCSB], [https://www.ebi.ac.uk/pdbsum/5yf4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5yf4 ProSAT]</span></td></tr> | 
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span></td></tr>
 | + |  | 
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5yf4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5yf4 OCA], [http://pdbe.org/5yf4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5yf4 RCSB], [http://www.ebi.ac.uk/pdbsum/5yf4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5yf4 ProSAT]</span></td></tr> | + |  | 
|  | </table> |  | </table> | 
|  | == Function == |  | == Function == | 
| - | [[http://www.uniprot.org/uniprot/PHOCN_HUMAN PHOCN_HUMAN]] May play a role in membrane trafficking, specifically in membrane budding reactions.[[http://www.uniprot.org/uniprot/STK26_HUMAN STK26_HUMAN]] Mediator of cell growth (PubMed:11641781, PubMed:17360971). Modulates apoptosis (PubMed:11641781, PubMed:17360971). In association with STK24 negatively regulates Golgi reorientation in polarized cell migration upon RHO activation (PubMed:27807006).<ref>PMID:11641781</ref> <ref>PMID:17360971</ref> <ref>PMID:27807006</ref>   | + | [https://www.uniprot.org/uniprot/PHOCN_HUMAN PHOCN_HUMAN] May play a role in membrane trafficking, specifically in membrane budding reactions. | 
|  | <div style="background-color:#fffaf0;"> |  | <div style="background-color:#fffaf0;"> | 
|  | == Publication Abstract from PubMed == |  | == Publication Abstract from PubMed == | 
| Line 25: | Line 23: | 
|  | __TOC__ |  | __TOC__ | 
|  | </StructureSection> |  | </StructureSection> | 
| - | [[Category: Human]] | + | [[Category: Homo sapiens]] | 
| - | [[Category: Non-specific serine/threonine protein kinase]] | + | [[Category: Large Structures]] | 
| - | [[Category: Chen, M]] | + | [[Category: Chen M]] | 
| - | [[Category: Zhou, Z C]] | + | [[Category: Zhou ZC]] | 
| - | [[Category: Complex]]
 | + |  | 
| - | [[Category: Kinase]]
 | + |  | 
| - | [[Category: Phosphorylation]]
 | + |  | 
| - | [[Category: Protein binding]]
 | + |  | 
|  |   Structural highlights   Function PHOCN_HUMAN May play a role in membrane trafficking, specifically in membrane budding reactions.
 
  Publication Abstract from PubMed The mammalian STE20-like protein kinase 1 (MST1)-MOB kinase activator 1 (MOB1) complex has been shown to suppress the oncogenic activity of Yes-associated protein (YAP) in the mammalian Hippo pathway, which is involved in the development of multiple tumors including pancreatic cancer (PC). However, it remains unclear whether other MST-MOB complexes are also involved in regulating Hippo-YAP signaling and have potential roles in PC. Here, we report that mammalian STE20-like kinase 4 (MST4), a distantly related ortholog of the MST1 kinase, forms a complex with MOB4 in a phosphorylation-dependent manner. We found that the overall structure of the MST4-MOB4 complex resembles that of the MST1-MOB1 complex, even though the two complexes exhibited opposite biological functions in PC. In contrast to the tumor-suppressor effect of the MST1-MOB1 complex, the MST4-MOB4 complex promoted growth and migration of PANC-1 cells. Moreover, expression levels of MST4 and MOB4 were elevated in PC and were positively correlated with each other, whereas MST1 expression was down-regulated. Owing to divergent evolution of key interface residues, MST4 and MOB4 could disrupt assembly of the MST1-MOB1 complex through alternative pairing and thereby increased YAP activity. Collectively, these findings identify the MST4-MOB4 complex as a noncanonical regulator of the Hippo-YAP pathway with an oncogenic role in PC. Our findings highlight that although MST-MOB complexes display some structural conservation, they functionally diverged during their evolution.
 The MST4-MOB4 complex disrupts the MST1-MOB1 complex in the Hippo-YAP pathway and plays a pro-oncogenic role in pancreatic cancer.,Chen M, Zhang H, Shi Z, Li Y, Zhang X, Gao Z, Zhou L, Ma J, Xu Q, Guan J, Cheng Y, Jiao S, Zhou Z J Biol Chem. 2018 Aug 2. pii: RA118.003279. doi: 10.1074/jbc.RA118.003279. PMID:30072378[1]
 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
   References ↑ Chen M, Zhang H, Shi Z, Li Y, Zhang X, Gao Z, Zhou L, Ma J, Xu Q, Guan J, Cheng Y, Jiao S, Zhou Z. The MST4-MOB4 complex disrupts the MST1-MOB1 complex in the Hippo-YAP pathway and plays a pro-oncogenic role in pancreatic cancer. J Biol Chem. 2018 Aug 2. pii: RA118.003279. doi: 10.1074/jbc.RA118.003279. PMID:30072378 doi:http://dx.doi.org/10.1074/jbc.RA118.003279
 
 |