2qfg | pdb_00002qfg
From Proteopedia
Solution Structure of the N-terminal SCR-1/5 fragment of Complement Factor H.
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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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
