2a73: Difference between revisions
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[[Image:2a73.gif|left|200px]] | [[Image:2a73.gif|left|200px]] | ||
'''Human Complement Component C3''' | {{Structure | ||
|PDB= 2a73 |SIZE=350|CAPTION= <scene name='initialview01'>2a73</scene>, resolution 3.30Å | |||
|SITE= | |||
|LIGAND= | |||
|ACTIVITY= | |||
|GENE= | |||
}} | |||
'''Human Complement Component C3''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
2A73 is a [ | 2A73 is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A73 OCA]. | ||
==Reference== | ==Reference== | ||
Structures of complement component C3 provide insights into the function and evolution of immunity., Janssen BJ, Huizinga EG, Raaijmakers HC, Roos A, Daha MR, Nilsson-Ekdahl K, Nilsson B, Gros P, Nature. 2005 Sep 22;437(7058):505-11. PMID:[http:// | Structures of complement component C3 provide insights into the function and evolution of immunity., Janssen BJ, Huizinga EG, Raaijmakers HC, Roos A, Daha MR, Nilsson-Ekdahl K, Nilsson B, Gros P, Nature. 2005 Sep 22;437(7058):505-11. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16177781 16177781] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: intact thioester]] | [[Category: intact thioester]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:46:09 2008'' | ||
Revision as of 16:46, 20 March 2008
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Human Complement Component C3
OverviewOverview
The mammalian complement system is a phylogenetically ancient cascade system that has a major role in innate and adaptive immunity. Activation of component C3 (1,641 residues) is central to the three complement pathways and results in inflammation and elimination of self and non-self targets. Here we present crystal structures of native C3 and its final major proteolytic fragment C3c. The structures reveal thirteen domains, nine of which were unpredicted, and suggest that the proteins of the alpha2-macroglobulin family evolved from a core of eight homologous domains. A double mechanism prevents hydrolysis of the thioester group, essential for covalent attachment of activated C3 to target surfaces. Marked conformational changes in the alpha-chain, including movement of a critical interaction site through a ring formed by the domains of the beta-chain, indicate an unprecedented, conformation-dependent mechanism of activation, regulation and biological function of C3.
DiseaseDisease
Known diseases associated with this structure: C3 deficiency OMIM:[120700], Macular degeneration, age-related, 9 OMIM:[120700]
About this StructureAbout this Structure
2A73 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
Structures of complement component C3 provide insights into the function and evolution of immunity., Janssen BJ, Huizinga EG, Raaijmakers HC, Roos A, Daha MR, Nilsson-Ekdahl K, Nilsson B, Gros P, Nature. 2005 Sep 22;437(7058):505-11. PMID:16177781
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