2qfg
From Proteopedia
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Solution Structure of the N-terminal SCR-1/5 fragment of Complement Factor H.
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
2QFG is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 23:32:47 2007
Categories: Homo sapiens | Single protein | Gilbert, H.E. | Gordon, D.L. | Griggs, K.M. | Okemefuna, A.I. | Ormsby, R.J. | Perkins, S.J. | Age-related macular degeneration | Alternative splicing | Complement | Complement alternate pathway | Disease mutation | Factor h | Glycoprotein | Immune response | Immune system | Innate immunity | Polymorphism | Scr domain | Sushi | X-ray scattering
