5ji7

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(New page: '''Unreleased structure''' The entry 5ji7 is ON HOLD Authors: Hong, S.K., Kim, K.-H., Kim, E.E. Description: Category: Unreleased Structures Category: Kim, K.-H [[Category: Ho...)
Current revision (09:17, 20 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5ji7 is ON HOLD
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==The Crystal Structure Of IUS-SPRY Domain From RanBPM/9==
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<StructureSection load='5ji7' size='340' side='right'caption='[[5ji7]], [[Resolution|resolution]] 1.51&Aring;' scene=''>
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Authors: Hong, S.K., Kim, K.-H., Kim, E.E.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ji7]] 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=5JI7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5JI7 FirstGlance]. <br>
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Description:
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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]] 1.51&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=5ji7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ji7 OCA], [https://pdbe.org/5ji7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5ji7 RCSB], [https://www.ebi.ac.uk/pdbsum/5ji7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5ji7 ProSAT]</span></td></tr>
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[[Category: Kim, K.-H]]
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</table>
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[[Category: Hong, S.K]]
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== Function ==
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[[Category: Kim, E.E]]
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[https://www.uniprot.org/uniprot/RANB9_HUMAN RANB9_HUMAN] May act as an adapter protein to couple membrane receptors to intracellular signaling pathways. May be involved in signaling of ITGB2/LFA-1 and other integrins. Enhances HGF-MET signaling by recruiting Sos and activating the Ras pathway. Enhances dihydrotestosterone-induced transactivation activity of AR, as well as dexamethasone-induced transactivation activity of NR3C1, but not affect estrogen-induced transactivation. Stabilizes TP73 isoform Alpha, probably by inhibiting its ubiquitination, and increases its proapoptotic activity. Inhibits the kinase activity of DYRK1A and DYRK1B. Inhibits FMR1 binding to RNA (By similarity).<ref>PMID:12147692</ref> <ref>PMID:12361945</ref> <ref>PMID:14500717</ref> <ref>PMID:14722085</ref> <ref>PMID:15381419</ref> <ref>PMID:15558019</ref> <ref>PMID:18222118</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: Hong SK]]
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[[Category: Kim EE]]
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[[Category: Kim K-H]]

Current revision

The Crystal Structure Of IUS-SPRY Domain From RanBPM/9

PDB ID 5ji7

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