Complement C5: Difference between revisions

From Proteopedia
Jump to navigationJump to search
No edit summary
Michal Harel (talk | contribs)
No edit summary
Line 8: Line 8:


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>


Line 27: Line 31:
**[[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  

Revision as of 06:37, 15 May 2019

Human complement C5 complex (green) with cobra venom factor (magenta) (PDB code 3pvm)

Drag the structure with the mouse to rotate

3D Structures of complement C5

Updated on 15-May-2019

References

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman