Complement component 2

C2
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2I6S, 3ERB,%%s2ODQ
Identifiers
Aliases	C2, ARMD14, CO2, complement component 2, complement C2
External IDs	OMIM: 613927 MGI: 88226 HomoloGene: 45 GeneCards: C2
Gene location (Human) Chr. Chromosome 6 (human) Band 6p21.33 Start 31,897,785 bp End 31,945,673 bp
Gene location (Mouse) Chr. Chromosome 17 (mouse) Band 17 B1|17 18.41 cM Start 35,081,580 bp End 35,117,241 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in liver right lobe of liver placenta spleen upper lobe of left lung gallbladder appendix right lung lymph node duodenum Top expressed in iris adrenal gland white adipose tissue left lobe of liver sciatic nerve ileum ciliary body subcutaneous adipose tissue carotid body uterine tube More reference expression data BioGPS More reference expression data
Gene ontology Molecular function peptidase activity serine-type peptidase activity hydrolase activity metal ion binding serine-type endopeptidase activity protein binding Cellular component extracellular region extracellular exosome extracellular space Biological process complement activation positive regulation of apoptotic cell clearance regulation of complement activation response to nutrient proteolysis complement activation, classical pathway immune system process innate immune response Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 717 12263 Ensembl ENSG00000206372 ENSG00000235017 ENSG00000235696 ENSG00000226560 ENSG00000204364 ENSG00000166278 ENSG00000231543 ENSMUSG00000024371 UniProt P06681 Q5JP69 P21180 RefSeq (mRNA) NM_000063 NM_001145903 NM_001178063 NM_001282457 NM_001282458 NM_001282459 NM_013484 RefSeq (protein) NP_000054 NP_001139375 NP_001171534 NP_001269386 NP_001269387 NP_001269388 NP_000054.2 NP_038512 Location (UCSC) Chr 6: 31.9 – 31.95 Mb Chr 17: 35.08 – 35.12 Mb PubMed search
Wikidata
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Complement C2 is a protein that in humans is encoded by the C2 gene. The protein encoded by this gene is part of the classical pathway of the complement system, acting as a multi-domain serine protease. Deficiency of C2 has been associated with certain autoimmune diseases.

Function

In the classical and lectin pathways of complement activation, formation of the C3-convertase and C5-convertases requires binding of C2 to an activated surface-bound C4b in the presence of Mg²⁺; the resultant C4bC2 complex is then cleaved by C1s or MASP2 into C2a and C2b. It is thought that cleavage of C2 by C1s, while bound to C4b, results in a conformational rotation of C2b whereas the released C2a fragment may retain most of its original structure.

C2b is the smallest , enzymatically active fragment which is incorporated into the C3 convertase in this pathway, C4b2b (NB: some sources now refer to the larger fragment of C2 as C2b, making the C3 convertase C4b2b, whereas older sources refer to the larger fragment of C2 as C2a, making the C3 convertase C4b2a). The smaller fragment, C2a (or C2b, depending on the source) is released into the fluid phase.

Further reading

• Bartholomew WR, Shanahan TC (1991). "Complement components and receptors: deficiencies and disease associations". Immunology Series. 52: 33–51. PMID 2091785.
• Campbell RD (Jan 1987). "The molecular genetics and polymorphism of C2 and factor B". British Medical Bulletin. 43 (1): 37–49. doi:10.1093/oxfordjournals.bmb.a072175. PMID 3315100.
• Yu CY (1999). "Molecular genetics of the human MHC complement gene cluster". Experimental and Clinical Immunogenetics. 15 (4): 213–230. doi:10.1159/000019075. PMID 10072631. S2CID 25061446.
• Lutsenko SM, Kharchenko VG, Bachurin VI, Lomakin MM (Feb 1976). "[Circulating blood volume and regional hemodynamics in acute gastrointestinal hemorrhage]". Sovetskaia Meditsina (2): 38–41. PMID 1084023.
• Zhu ZB, Hsieh SL, Bentley DR, Campbell RD, Volanakis JE (Jun 1992). "A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus". The Journal of Experimental Medicine. 175 (6): 1783–1787. doi:10.1084/jem.175.6.1783. PMC 2119228. PMID 1350302.
• Lappin DF, Guc D, Hill A, McShane T, Whaley K (Jan 1992). "Effect of interferon-gamma on complement gene expression in different cell types". The Biochemical Journal. 281 (Pt 2): 437–442. doi:10.1042/bj2810437. PMC 1130704. PMID 1531292.
• Johnson CA, Densen P, Hurford RK, Colten HR, Wetsel RA (May 1992). "Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing". The Journal of Biological Chemistry. 267 (13): 9347–9353. PMID 1577763.
• Hasans dropping fat logs Lappin DF, Birnie GD, Whaley K (Nov 1990). "Interferon-mediated transcriptional and post-transcriptional modulation of complement gene expression in human monocytes". European Journal of Biochemistry / FEBS. 194 (1): 177–184. doi:10.1111/j.1432-1033.1990.tb19443.x. PMID 1701385.
• Horiuchi T, Macon KJ, Kidd VJ, Volanakis JE (Mar 1989). "cDNA cloning and expression of human complement component C2". Journal of Immunology. 142 (6): 2105–2111. PMID 2493504.
• Cole FS, Whitehead AS, Auerbach HS, Lint T, Zeitz HJ, Kilbridge P, Colten HR (Jul 1985). "The molecular basis for genetic deficiency of the second component of human complement". The New England Journal of Medicine. 313 (1): 11–16. doi:10.1056/NEJM198507043130103. PMID 2582254.
• Bentley DR (Oct 1986). "Primary structure of human complement component C2. Homology to two unrelated protein families". The Biochemical Journal. 239 (2): 339–345. doi:10.1042/bj2390339. PMC 1147286. PMID 2949737.
• Bentley DR, Campbell RD, Cross SJ (1985). "DNA polymorphism of the C2 locus". Immunogenetics. 22 (4): 377–390. doi:10.1007/BF00430921. PMID 2997031. S2CID 11934813.
• Kam CM, McRae BJ, Harper JW, Niemann MA, Volanakis JE, Powers JC (Mar 1987). "Human complement proteins D, C2, and B. Active site mapping with peptide thioester substrates". The Journal of Biological Chemistry. 262 (8): 3444–3451. PMID 3546307.
• Wu LC, Morley BJ, Campbell RD (Jan 1987). "Cell-specific expression of the human complement protein factor B gene: evidence for the role of two distinct 5'-flanking elements". Cell. 48 (2): 331–342. doi:10.1016/0092-8674(87)90436-3. PMID 3643061. S2CID 32752642.
• Gagnon J (Sep 1984). "Structure and activation of complement components C2 and factor B". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 306 (1129): 301–309. Bibcode:1984RSPTB.306..301G. doi:10.1098/rstb.1984.0091. PMID 6149575.
• Bentley DR, Porter RR (Feb 1984). "Isolation of cDNA clones for human complement component C2". Proceedings of the National Academy of Sciences of the United States of America. 81 (4): 1212–1215. Bibcode:1984PNAS...81.1212B. doi:10.1073/pnas.81.4.1212. PMC 344796. PMID 6199794.
• Parkes C, Gagnon J, Kerr MA (Jul 1983). "The reaction of iodine and thiol-blocking reagents with human complement components C2 and factor B. Purification and N-terminal amino acid sequence of a peptide from C2a containing a free thiol group". The Biochemical Journal. 213 (1): 201–209. doi:10.1042/bj2130201. PMC 1152109. PMID 6555044.
• Kerr MA, Gagnon J (Jul 1982). "The purification and properties of the second component of guinea-pig complement". The Biochemical Journal. 205 (1): 59–67. doi:10.1042/bj2050059. PMC 1158446. PMID 6922702.

External links

• Complement+2 at the U.S. National Library of Medicine Medical Subject Headings (MeSH)