This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
8ptl
From Proteopedia
(Difference between revisions)
m (Protected "8ptl" [edit=sysop:move=sysop]) |
|||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==human PHOX2B C-terminal domain including the polyA fragment at 278K== | |
| - | + | <StructureSection load='8ptl' size='340' side='right'caption='[[8ptl]]' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8ptl]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8PTL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8PTL 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> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8ptl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ptl OCA], [https://pdbe.org/8ptl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ptl RCSB], [https://www.ebi.ac.uk/pdbsum/8ptl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ptl ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/PHX2B_HUMAN PHX2B_HUMAN] Neuroblastoma;Congenital central hypoventilation syndrome;Hirschsprung disease-ganglioneuroblastoma syndrome;Haddad syndrome. The disease is caused by variants affecting the gene represented in this entry. Disease susceptibility is associated with variants affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/PHX2B_HUMAN PHX2B_HUMAN] Involved in the development of several major noradrenergic neuron populations, including the locus coeruleus. Transcription factor which could determine a neurotransmitter phenotype in vertebrates. Enhances second-messenger-mediated activation of the dopamine beta-hydrolase and c-fos promoters, and of several enhancers including cAMP-response element and serum-response element. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Anton R]] | ||
| + | [[Category: Babu M]] | ||
| + | [[Category: Cabrita EJ]] | ||
| + | [[Category: Felix S]] | ||
| + | [[Category: Oroz J]] | ||
| + | [[Category: Pantoja-Uceda D]] | ||
| + | [[Category: Tinnefeld P]] | ||
| + | [[Category: Trevino MA]] | ||
| + | [[Category: Vera AM]] | ||
| + | [[Category: Zweckstetter M]] | ||
Current revision
human PHOX2B C-terminal domain including the polyA fragment at 278K
| |||||||||||
Categories: Homo sapiens | Large Structures | Anton R | Babu M | Cabrita EJ | Felix S | Oroz J | Pantoja-Uceda D | Tinnefeld P | Trevino MA | Vera AM | Zweckstetter M
