3k1r

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
+
{{Seed}}
 +
[[Image:3k1r.jpg|left|200px]]
-
The entry 3k1r is ON HOLD until Paper Publication
+
<!--
 +
The line below this paragraph, containing "STRUCTURE_3k1r", 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_3k1r| PDB=3k1r | SCENE= }}
-
Authors: Pan, L., Yan, J., Zhang, M.
+
===Structure of harmonin NPDZ1 in complex with the SAM-PBM of Sans===
-
Description: Structure of harmonin NPDZ1 in complex with the SAM-PBM of Sans
 
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 21 10:00:15 2009''
+
==Disease==
 +
Known disease associated with this structure: Deafness, autosomal recessive 18 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605242 605242]], Usher syndrome, type 1C OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605242 605242]], Usher syndrome, type 1G OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=607696 607696]]
 +
 
 +
==About this Structure==
 +
3K1R is a 2 chains structure with sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3K1R OCA].
 +
[[Category: Homo sapiens]]
 +
[[Category: Pan, L.]]
 +
[[Category: Yan, J.]]
 +
[[Category: Zhang, M.]]
 +
[[Category: Alternative splicing]]
 +
[[Category: Ank repeat]]
 +
[[Category: Coiled coil]]
 +
[[Category: Deafness]]
 +
[[Category: Disease mutation]]
 +
[[Category: Hearing]]
 +
[[Category: Non-syndromic deafness]]
 +
[[Category: Polymorphism]]
 +
[[Category: Protein-protein complex]]
 +
[[Category: Retinitis pigmentosa]]
 +
[[Category: Sensory transduction]]
 +
[[Category: Structural protein]]
 +
[[Category: Usher syndrome]]
 +
[[Category: Vision]]
 +
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 27 20:02:05 2010''

Revision as of 18:02, 27 January 2010

Image:3k1r.jpg

Template:STRUCTURE 3k1r

Structure of harmonin NPDZ1 in complex with the SAM-PBM of Sans

Disease

Known disease associated with this structure: Deafness, autosomal recessive 18 OMIM:[605242], Usher syndrome, type 1C OMIM:[605242], Usher syndrome, type 1G OMIM:[607696]

About this Structure

3K1R is a 2 chains structure with sequences from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Wed Jan 27 20:02:05 2010

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/3k1r"
Personal tools