Complement C5: Difference between revisions
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Mutations in CC5 cause a deficiency leading to severe recurrent infections and are linked to liver fibrosis, Leiner's disease and rheumatoid arthritis. | Mutations in CC5 cause a deficiency leading to severe recurrent infections and are linked to liver fibrosis, Leiner's disease and rheumatoid arthritis. | ||
== 3D Structures of complement C5 == | |||
[[Complement C5 3D structures]] | |||
</StructureSection> | </StructureSection> | ||
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**[[5hcd]] – hCC5 + complement inhibitor + RACI2<BR /> | **[[5hcd]] – hCC5 + complement inhibitor + RACI2<BR /> | ||
**[[5hce]] – hCC5 + complement inhibitor + RACI1<BR /> | **[[5hce]] – hCC5 + complement inhibitor + RACI1<BR /> | ||
**[[6h04]] – hCC5 + hCC9 + hCC8 a+b+g chains + hCC7 – Cryo EM<BR /> | |||
*C345C | *C345C | ||
