2xqw: Difference between revisions
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:021285368</ref><ref group="xtra">PMID:016601698</ref><ref group="xtra">PMID:019351878</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bhattacharjee, A.]] | [[Category: Bhattacharjee, A.]] | ||
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[[Category: Leung, E.]] | [[Category: Leung, E.]] | ||
[[Category: Meri, S.]] | [[Category: Meri, S.]] | ||
[[Category: Ahus]] | |||
[[Category: Atypical hemolytic uremic syndrome]] | |||
[[Category: C3b]] | |||
[[Category: Cfh]] | |||
[[Category: Complement alternative pathway]] | |||
[[Category: Fh]] | |||
[[Category: Immune system]] | |||
Revision as of 09:39, 17 August 2011
STRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3DSTRUCTURE OF FACTOR H DOMAINS 19-20 IN COMPLEX WITH COMPLEMENT C3D
Template:ABSTRACT PUBMED 21285368
About this StructureAbout this Structure
2xqw is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ 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