4gei: Difference between revisions

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'''Unreleased structure'''


The entry 4gei is ON HOLD
==N-terminal domain of VDUP-1==
 
<StructureSection load='4gei' size='340' side='right'caption='[[4gei]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
Authors: Polekhina, G., Kok, S. F., Ascher, D. B., Waltham, M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[4gei]] 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=4GEI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4GEI FirstGlance]. <br>
Description: N-terminal domain of VDUP-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]] 1.5&#8491;</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=4gei FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gei OCA], [https://pdbe.org/4gei PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4gei RCSB], [https://www.ebi.ac.uk/pdbsum/4gei PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4gei ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/TXNIP_HUMAN TXNIP_HUMAN] May act as an oxidative stress mediator by inhibiting thioredoxin activity or by limiting its bioavailability. Interacts with COPS5 and restores COPS5-induced suppression of CDKN1B stability, blocking the COPS5-mediated translocation of CDKN1B from the nucleus to the cytoplasm. Functions as a transcriptional repressor, possibly by acting as a bridge molecule between transcription factors and corepressor complexes, and over-expression will induce G0/G1 cell cycle arrest. Required for the maturation of natural killer cells. Acts as a suppressor of tumor cell growth. Inhibits the proteasomal degradation of DDIT4, and thereby contributes to the inhibition of the mammalian target of rapamycin complex 1 (mTORC1).<ref>PMID:17603038</ref> <ref>PMID:12821938</ref> <ref>PMID:18541147</ref> <ref>PMID:21460850</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ascher DB]]
[[Category: Kok SF]]
[[Category: Polekhina G]]
[[Category: Waltham M]]

Latest revision as of 11:28, 1 March 2024

N-terminal domain of VDUP-1

4gei, resolution 1.50Å

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