8ia5: Difference between revisions

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-'''Unreleased structure'''
-The entry 8ia5 is ON HOLD
+==Small peptide enhances the binding of nutline-3a to N-terminal domain of MdmX==
+<StructureSection load='8ia5' size='340' side='right'caption='[[8ia5]], [[Resolution|resolution]] 1.93&Aring;' scene=''>
-Authors: Cheng, X.Y., Wei, Q.Y., Huang, Y., Su, Z.D.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8ia5]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8IA5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8IA5 FirstGlance]. <br>
-Description: Small peptide enhances the binding of nutline-3a to N-terminal domain of MdmX
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NUT:4-({(4S,5R)-4,5-BIS(4-CHLOROPHENYL)-2-[4-METHOXY-2-(PROPAN-2-YLOXY)PHENYL]-4,5-DIHYDRO-1H-IMIDAZOL-1-YL}CARBONYL)PIPERAZIN-2-ONE'>NUT</scene>, <scene name='pdbligand=O4B:1,4,7,10,13,16-HEXAOXACYCLOOCTADECANE'>O4B</scene></td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8ia5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ia5 OCA], [https://pdbe.org/8ia5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ia5 RCSB], [https://www.ebi.ac.uk/pdbsum/8ia5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ia5 ProSAT]</span></td></tr>
-[[Category: Su, Z.D]]
+</table>
-[[Category: Huang, Y]]
+== Function ==
-[[Category: Cheng, X.Y]]
+[https://www.uniprot.org/uniprot/MDM4_HUMAN MDM4_HUMAN] Inhibits p53/TP53- and TP73/p73-mediated cell cycle arrest and apoptosis by binding its transcriptional activation domain. Inhibits degradation of MDM2. Can reverse MDM2-targeted degradation of TP53 while maintaining suppression of TP53 transactivation and apoptotic functions.<ref>PMID:16163388</ref> <ref>PMID:16511572</ref>
-[[Category: Wei, Q.Y]]
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Synthetic construct]]
+[[Category: Cheng XY]]
+[[Category: Huang Y]]
+[[Category: Su ZD]]
+[[Category: Wei QY]]