9gkf

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (10:24, 3 September 2025) (edit) (undo)
 
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 9gkf is ON HOLD until Paper Publication
+
==Amyloid Fibril of Heterogeneous nuclear ribonucleoprotein A1A induced by RNA binding==
-
 
+
<StructureSection load='9gkf' size='340' side='right'caption='[[9gkf]], [[Resolution|resolution]] 3.21&Aring;' scene=''>
-
Authors: Frey, L., Riek, R.P., Arosio, P., Morelli, C.
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[9gkf]] is a 20 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=9GKF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9GKF FirstGlance]. <br>
-
Description: Amyloid Fibril of Heterogeneous nuclear ribonucleoprotein A1A induced by RNA binding
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.21&#8491;</td></tr>
-
[[Category: Unreleased Structures]]
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9gkf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9gkf OCA], [https://pdbe.org/9gkf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9gkf RCSB], [https://www.ebi.ac.uk/pdbsum/9gkf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9gkf ProSAT]</span></td></tr>
-
[[Category: Arosio, P]]
+
</table>
-
[[Category: Riek, R.P]]
+
== Disease ==
-
[[Category: Morelli, C]]
+
[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>
-
[[Category: Frey, L]]
+
== 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: Arosio P]]
 +
[[Category: Frey L]]
 +
[[Category: Morelli C]]
 +
[[Category: Riek RP]]

Current revision

Amyloid Fibril of Heterogeneous nuclear ribonucleoprotein A1A induced by RNA binding

PDB ID 9gkf

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/9gkf"
Personal tools