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4gei

From Proteopedia

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[[Image:4gei.jpg|left|200px]]
 
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{{STRUCTURE_4gei| PDB=4gei | SCENE= }}
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==N-terminal domain of VDUP-1==
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<StructureSection load='4gei' size='340' side='right'caption='[[4gei]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
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===N-terminal domain of VDUP-1===
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== Structural highlights ==
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<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>
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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]] 1.5&#8491;</td></tr>
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==About this Structure==
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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=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>
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[[4gei]] is a 1 chain structure with sequence from [http://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].
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</table>
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== Function ==
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[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Ascher, D B.]]
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[[Category: Large Structures]]
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[[Category: Kok, S F.]]
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[[Category: Ascher DB]]
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[[Category: Polekhina, G.]]
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[[Category: Kok SF]]
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[[Category: Waltham, M.]]
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[[Category: Polekhina G]]
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[[Category: Alpha-arrestin]]
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[[Category: Waltham M]]
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[[Category: Metabolism]]
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[[Category: Oxidative stress]]
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[[Category: Protein binding]]
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[[Category: Thioredoxin]]
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Current revision

N-terminal domain of VDUP-1

PDB ID 4gei

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