2xqw

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
+
[[Image:2xqw.jpg|left|200px]]
-
The entry 2xqw is ON HOLD until Paper Publication
+
<!--
 +
The line below this paragraph, containing "STRUCTURE_2xqw", 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_2xqw| PDB=2xqw | SCENE= }}
-
Authors: Kajander, T., Lehtinen, M.J., Hyvarinen, S., Bhattacharjee, A., Jokiranta, T.S., Goldman, A.
+
===STRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3D===
-
Description: Structure of Factor H domains 19-20 in complex with complement C3d
 
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Nov 3 09:56:13 2010''
+
==About this Structure==
 +
[[2xqw]] is a 3 chain structure with sequence 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=2XQW OCA].
 +
 
 +
==Reference==
 +
<ref group="xtra">PMID:16601698</ref><ref group="xtra">PMID:19351878</ref><references group="xtra"/>
 +
[[Category: Homo sapiens]]
 +
[[Category: Bhattacharjee, A.]]
 +
[[Category: Goldman, A.]]
 +
[[Category: Hyvarinen, S.]]
 +
[[Category: Isenman, D E.]]
 +
[[Category: Jokiranta, T S.]]
 +
[[Category: Kajander, T.]]
 +
[[Category: Lehtinen, M J.]]
 +
[[Category: Leung, E.]]
 +
[[Category: Meri, S.]]

Revision as of 06:26, 2 February 2011

Template:STRUCTURE 2xqw

STRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3D

About this Structure

2xqw is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Jokiranta TS, Jaakola VP, Lehtinen MJ, Parepalo M, Meri S, Goldman A. Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome. EMBO J. 2006 Apr 19;25(8):1784-94. Epub 2006 Apr 6. PMID:16601698
  • Lehtinen MJ, Rops AL, Isenman DE, van der Vlag J, Jokiranta TS. Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome. J Biol Chem. 2009 Jun 5;284(23):15650-8. Epub 2009 Apr 7. PMID:19351878 doi:10.1074/jbc.M900814200

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools