2k27: Difference between revisions

Revision as of 21:33, 1 October 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:2k27.jpg

Template:STRUCTURE 2k27

Solution structure of Human Pax8 Paired Box DomainSolution structure of Human Pax8 Paired Box Domain

DiseaseDisease

Known disease associated with this structure: Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia OMIM:[167415]

About this StructureAbout this Structure

2K27 is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.

Page seeded by OCA on Wed Oct 1 21:33:05 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{Seed}}
+[[Image:2k27.jpg|left|200px]]
-The entry 2k27 is ON HOLD  until Paper Publication
+<!--
+The line below this paragraph, containing "STRUCTURE_2k27", creates the "Structure Box" on the page.
+You may change the PDB parameter (which sets the PDB file loaded into the applet)
+or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+or leave the SCENE parameter empty for the default display.
+-->
+{{STRUCTURE_2k27|  PDB=2k27  |  SCENE=  }}
-Authors: Codutti, L., Esposito, G., Corazza, A., Fogolari, F., Tell, G., Vascotto, C., van Ingen, H., Boelens, R., Viglino, P., Quadrifoglio, F.
+===Solution structure of Human Pax8 Paired Box Domain===
-Description: Solution structure of Human Pax8 Paired Box Domain
+==Disease==
+Known disease associated with this structure: Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167415 167415]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 11 08:36:28 2008''
+==About this Structure==
+K27 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2K27 OCA].
+[[Category: Homo sapiens]]
+[[Category: Single protein]]
+[[Category: Boelens, R.]]
+[[Category: Codutti, L.]]
+[[Category: Corazza, A.]]
+[[Category: Esposito, G.]]
+[[Category: Fogolari, F.]]
+[[Category: Ingen, H van.]]
+[[Category: Quadrifoglio, F.]]
+[[Category: Tell, G.]]
+[[Category: Vascotto, C.]]
+[[Category: Viglino, P.]]
+[[Category: 3d nmr]]
+[[Category: Alternative splicing]]
+[[Category: Developmental protein]]
+[[Category: Differentiation]]
+[[Category: Disease mutation]]
+[[Category: Dna-binding]]
+[[Category: Induced fit]]
+[[Category: Nmr]]
+[[Category: Nucleus]]
+[[Category: Paired box]]
+[[Category: Paired domain]]
+[[Category: Pax8]]
+[[Category: Phosphoprotein]]
+[[Category: Polymorphism]]
+[[Category: Solution structure]]
+[[Category: Transcription]]
+[[Category: Transcription regulation]]
+[[Category: Transcription regulator]]
+[[Category: Triple frequency]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct  1 21:33:05 2008''