2l2k: Difference between revisions

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New page: '''Unreleased structure''' The entry 2l2k is ON HOLD Authors: Allain, F.H.-T., Oberstrass, F.C., Stefl, R. Description: Solution NMR structure of the R/G STEM LOOP RNA-ADAR2 DSRBM2 Com...
 
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'''Unreleased structure'''


The entry 2l2k is ON HOLD
==Solution NMR structure of the R/G STEM LOOP RNA-ADAR2 DSRBM2 Complex==
<StructureSection load='2l2k' size='340' side='right'caption='[[2l2k]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2l2k]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L2K OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L2K FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2l2k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l2k OCA], [https://pdbe.org/2l2k PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l2k RCSB], [https://www.ebi.ac.uk/pdbsum/2l2k PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l2k ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/RED1_MOUSE RED1_MOUSE] Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. Can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2 and GRIK2) and serotonin (HTR2C), GABA receptor (GABRA3) and potassium voltage-gated channel (KCNA1). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alter their functional activities. Edits GRIA2 at both the Q/R and R/G sites efficiently but converts the adenosine in hotspot1 much less efficiently. Can inhibit cell proliferation and migration and can stimulate exocytosis.<ref>PMID:17369310</ref>


Authors: Allain, F.H.-T., Oberstrass, F.C., Stefl, R.
==See Also==
 
*[[Adenosine deaminase 3D structures|Adenosine deaminase 3D structures]]
Description: Solution NMR structure of the R/G STEM LOOP RNA-ADAR2 DSRBM2 Complex
== References ==
 
<references/>
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep  1 09:27:51 2010''
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Allain FH-T]]
[[Category: Oberstrass FC]]
[[Category: Stefl R]]

Latest revision as of 06:51, 1 May 2024

Solution NMR structure of the R/G STEM LOOP RNA-ADAR2 DSRBM2 Complex

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