2jgw | pdb_00002jgw
From Proteopedia
STRUCTURE OF CCP MODULE 7 OF COMPLEMENT FACTOR H- THE AMD AT RISK VARIENT (402H)
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| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
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
2JGW 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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
