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.


7qqe

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 7qqe is ON HOLD until Paper Publication
+
==Nuclear factor one X - NFIX in P41212==
-
 
+
<StructureSection load='7qqe' size='340' side='right'caption='[[7qqe]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
-
Authors:
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[7qqe]] 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=7QQE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7QQE FirstGlance]. <br>
-
Description:
+
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EPE:4-(2-HYDROXYETHYL)-1-PIPERAZINE+ETHANESULFONIC+ACID'>EPE</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=7qqe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7qqe OCA], [https://pdbe.org/7qqe PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7qqe RCSB], [https://www.ebi.ac.uk/pdbsum/7qqe PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7qqe ProSAT]</span></td></tr>
 +
</table>
 +
== Disease ==
 +
[https://www.uniprot.org/uniprot/NFIX_HUMAN NFIX_HUMAN] 19p13.3 microduplication syndrome;Malan overgrowth syndrome;Marshall-Smith syndrome. 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/NFIX_HUMAN NFIX_HUMAN] Recognizes and binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and in the origin of replication of adenovirus type 2. These proteins are individually capable of activating transcription and replication.
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Homo sapiens]]
 +
[[Category: Large Structures]]
 +
[[Category: Bais G]]
 +
[[Category: Chaves-Sanjuan A]]
 +
[[Category: Demitri N]]
 +
[[Category: Gourlay LJ]]
 +
[[Category: Lapi M]]
 +
[[Category: Nardini M]]
 +
[[Category: Polentarutti M]]
 +
[[Category: Tiberi M]]

Revision as of 07:12, 18 January 2023

Nuclear factor one X - NFIX in P41212

PDB ID 7qqe

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools