View source for 8ter


==Tropomyosin-receptor kinase fused gene protein (TRK-fused gene protein; TFG) Low Complexity Domain (residues 237-327) P285L mutant, amyloid fiber==
<StructureSection load='8ter' size='340' side='right'caption='[[8ter]], [[Resolution|resolution]] 2.59&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8ter]] is a 20 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Purpureocillium_lilacinum Purpureocillium lilacinum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8TER OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8TER FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.59&#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=8ter FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ter OCA], [https://pdbe.org/8ter PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ter RCSB], [https://www.ebi.ac.uk/pdbsum/8ter PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ter ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/TFG_HUMAN TFG_HUMAN] Autosomal recessive spastic paraplegia type 57;Extraskeletal myxoid chondrosarcoma;Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation;Hereditary motor and sensory neuropathy, Okinawa type;Differentiated thyroid carcinoma. A chromosomal aberration involving TFG is found in papillary thyroid carcinomas (PTCs). Translocation t(1;3)(q21;q11) with NTRK1. The TFG sequence is fused to the 3'-end of NTRK1 generating the TRKT3 (TRK-T3) fusion transcript.<ref>PMID:7565764</ref>   The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/TFG_HUMAN TFG_HUMAN] Plays a role in the normal dynamic function of the endoplasmic reticulum (ER) and its associated microtubules (PubMed:23479643, PubMed:27813252). Required for secretory cargo traffic from the endoplasmic reticulum to the Golgi apparatus (PubMed:21478858).<ref>PMID:21478858</ref> <ref>PMID:23479643</ref> <ref>PMID:27813252</ref> [https://www.uniprot.org/uniprot/A0A2U3DNX3_PURLI A0A2U3DNX3_PURLI] 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Purpureocillium lilacinum]]
[[Category: Abskharon R]]
[[Category: Boyer DR]]
[[Category: Eisenberg DS]]
[[Category: Ge P]]
[[Category: Rosenberg GM]]
[[Category: Sawaya MR]]