9f4m: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
m Protected "9f4m" [edit=sysop:move=sysop]
OCA (talk | contribs)
No edit summary
 
Line 1: Line 1:
'''Unreleased structure'''


The entry 9f4m is ON HOLD
==UP1 in complex with Z1401276297==
 
<StructureSection load='9f4m' size='340' side='right'caption='[[9f4m]], [[Resolution|resolution]] 1.39&Aring;' scene=''>
Authors: Dunnett, L., Prischi, F.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9f4m]] 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=9F4M OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9F4M FirstGlance]. <br>
Description: UP1 in complex with Z1401276297
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.39&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1H97:(5~{R})-7-pyrazin-2-yl-2-oxa-7-azaspiro[4.4]nonane'>A1H97</scene></td></tr>
[[Category: Prischi, F]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9f4m FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9f4m OCA], [https://pdbe.org/9f4m PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9f4m RCSB], [https://www.ebi.ac.uk/pdbsum/9f4m PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9f4m ProSAT]</span></td></tr>
[[Category: Dunnett, L]]
</table>
== Disease ==
[https://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN] Amyotrophic lateral sclerosis;Inclusion body myopathy with Paget disease of bone and frontotemporal dementia. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref>  The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref>
== Function ==
[https://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN] Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection. May play a role in HCV RNA replication.<ref>PMID:17229681</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Dunnett L]]
[[Category: Prischi F]]

Latest revision as of 05:29, 15 May 2024

UP1 in complex with Z1401276297

9f4m, resolution 1.39Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA