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2xqw

From Proteopedia

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===STRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3D===
===STRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3D===
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(as it appears on PubMed at http://www.pubmed.gov), where 21285368 is the PubMed ID number.
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{{ABSTRACT_PUBMED_21285368}}
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
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<ref group="xtra">PMID:16601698</ref><ref group="xtra">PMID:19351878</ref><references group="xtra"/>
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<ref group="xtra">PMID:21285368</ref><ref group="xtra">PMID:16601698</ref><ref group="xtra">PMID:19351878</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Bhattacharjee, A.]]
[[Category: Bhattacharjee, A.]]

Revision as of 05:05, 16 February 2011

Image:2xqw.png

Template:STRUCTURE 2xqw

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

Template:ABSTRACT PUBMED 21285368

About this Structure

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

Reference

  • Kajander T, Lehtinen MJ, Hyvarinen S, Bhattacharjee A, Leung E, Isenman DE, Meri S, Goldman A, Jokiranta TS. Dual interaction of factor H with C3d and glycosaminoglycans in host-nonhost discrimination by complement. Proc Natl Acad Sci U S A. 2011 Feb 1. PMID:21285368 doi:10.1073/pnas.1017087108
  • 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

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OCA

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