2jgx
From Proteopedia
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STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD NOT AT RISK VARIENT (402Y)
Disease
Known diseases associated with this structure: Complement factor H deficiency OMIM:[134370], Factor H and factor H-like 1 OMIM:[134370], Hemolytic-uremic syndrome OMIM:[134370], Macular degeneration, age-related, 4 OMIM:[134370], Membranoproliferative glomerulonephritis with CFH deficiency OMIM:[134370]
About this Structure
2JGX is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Mar 20 17:41:44 2008
Categories: Homo sapiens | Single protein | Barlow, P N. | Blaum, B S. | Deakin, J A. | Egan, C. | Ferreira, V P. | Herbert, A P. | Lyon, M. | Pangburn, M K. | Schmidt, C Q. | Uhrin, D. | Age related macular degeneration | Age-related macular degeneration | Alternative splicing | Complement | Complement alternate pathway | Disease mutation | Factor h | Glycoprotein | Glycosaminoglycan | Immune response | Innate immunity | Polymorphism | Sushi
