Complement C5: Difference between revisions

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<StructureSection load='3pvm' size='340' side='right' caption='Human complement C5 complex (grey and pink) with cobra venom factor (green and yellow) (PDB code [[3pvm]])' scene=''>
<StructureSection load='3pvm' size='340' side='right' caption='Human complement C5 complex (grey and pink) with cobra venom factor (green and yellow) (PDB code [[3pvm]])' scene=''>
'''Complement C5''' (CC5) is the fifth component of the complement system.  The complement system is part of the innate immune system.  CC5 is composed of α chain (C5a) and β chain (C5b).  Proteoplytic degradation of CC5 produces '''anaphylatoxin''' which is a mediator of local inflammatory process.  The C terminal domain of CC5 (residues 1530-1676) is homologous to a domain in netrins and is named '''C345C'''.  Activation of CC5 by C5 convertase initiates the assembly of the C5 to C9 components into the membrane attack complex.
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== Function ==


== Function ==
'''Complement C5''' (CC5) is the fifth component of the complement system.  The complement system is part of the innate immune system.  CC5 is composed of α chain (C5a) and β chain (C5b).  Proteoplytic degradation of CC5 produces '''anaphylatoxin''' which is a mediator of local inflammatory process.  The C terminal domain of CC5 (residues 1530-1676) is homologous to a domain in netrins and is named '''C345C'''.  Activation of CC5 by C5 convertase initiates the assembly of the C5 to C9 components into the membrane attack complex. <ref>PMID:18536718</ref>


== Disease ==
== Disease ==


Mutations in CC5 cause a deficiency leading to severe recurrent infections and are linked to liver fibrosis 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.
 
== Relevance ==
 
== Structural highlights ==
 
 
</StructureSection>
</StructureSection>