2l7f

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
m (Protected "2l7f" [edit=sysop:move=sysop])
Line 1: Line 1:
-
[[Image:2l7f.jpg|left|200px]]
+
==Solution Structure of the Pitx2 Homeodomain==
-
 
+
<StructureSection load='2l7f' size='340' side='right' caption='[[2l7f]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
-
<!--
+
== Structural highlights ==
-
The line below this paragraph, containing "STRUCTURE_2l7f", creates the "Structure Box" on the page.
+
[[2l7f]] is a 1 chain structure with 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=2L7F OCA]. <br>
-
You may change the PDB parameter (which sets the PDB file loaded into the applet)
+
<b>Activity:</b> <span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span><br>
-
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+
== Disease ==
-
or leave the SCENE parameter empty for the default display.
+
[[http://www.uniprot.org/uniprot/PITX2_HUMAN PITX2_HUMAN]] Peters anomaly;Axenfeld anomaly;Rieger anomaly;Ring dermoid of cornea;Axenfeld-Rieger syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
-
-->
+
== Function ==
-
{{STRUCTURE_2l7f| PDB=2l7f | SCENE= }}
+
[[http://www.uniprot.org/uniprot/PITX2_HUMAN PITX2_HUMAN]] Controls cell proliferation in a tissue-specific manner and is involved in morphogenesis. During embryonic development, exerts a role in the expansion of muscle progenitors. May play a role in the proper localization of asymmetric organs such as the heart and stomach. Isoform PTX2C is involved in left-right asymmetry the developing embryo (By similarity).
-
 
+
== References ==
-
===Solution Structure of the Pitx2 Homeodomain===
+
<references/>
-
 
+
__TOC__
-
 
+
</StructureSection>
-
==About this Structure==
+
-
[[2l7f]] is a 1 chain structure with 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=2L7F OCA].
+
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Baird-Titus, J M.]]
[[Category: Baird-Titus, J M.]]

Revision as of 08:31, 30 April 2014

Solution Structure of the Pitx2 Homeodomain

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/2l7f"
Personal tools