C5
WordNet
- make complete or perfect; supply what is wanting or form the complement to; "I need some pepper to complement the sweet touch in the soup"
- a complete number or quantity; "a full complement"
- one of a series of enzymes in the blood serum that are part of the immune response
- something added to complete or embellish or make perfect; "a fine wine is a perfect complement to the dinner"; "wild rice was served as an accompaniment to the main dish" (同)accompaniment
- number needed to make up a whole force; "a full complement of workers" (同)full complement
- a word or phrase used to complete a grammatical construction
- either of two parts that mutually complete each other
- an artifact that is one of the individual parts of which a composite entity is made up; especially a part that can be separated from or attached to a system; "spare components for cars"; "a component or constituent element of a system" (同)constituent, element
- an abstract part of something; "jealousy was a component of his character"; "two constituents of a musical composition are melody and harmony"; "the grammatical elements of a sentence"; "a key factor in her success"; "humor: an effective ingredient of a s (同)constituent, element, factor, ingredient
PrepTutorEJDIC
- (あるものを完全にするため)(…を)補う物(事)《+『of』+『名』》 / 補語(文法で文の成分の一つ) / (必要な)全数,全量;(船の)定員 / …を補足する,補う
- 構成している,成分の / 構成要素,成分
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2018/03/21 07:08:40」(JST)
[Wiki en表示]
C5 |
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Available structures |
PDB |
Ortholog search: PDBe RCSB |
List of PDB id codes |
1CFA, 1KJS, 1XWE, 3CU7, 3HQA, 3HQB, 3KLS, 3KM9, 3PRX, 3PVM, 4A5W, 4E0S, 4P39, 4UU9, 5I5K, 5HCE, 5HCC, 5HCD
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Identifiers |
Aliases |
C5, C5D, C5a, C5b, CPAMD4, ECLZB, complement component 5, complement C5 |
External IDs |
OMIM: 120900 MGI: 96031 HomoloGene: 20412 GeneCards: C5 |
Gene location (Human) |
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Chr. |
Chromosome 9 (human)[1] |
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Band |
9q33.2 |
Start |
120,952,335 bp[1] |
End |
121,050,276 bp[1] |
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Gene location (Mouse) |
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Chr. |
Chromosome 2 (mouse)[2] |
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Band |
2 B|2 23.22 cM |
Start |
34,983,331 bp[2] |
End |
35,061,438 bp[2] |
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RNA expression pattern |
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More reference expression data |
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Gene ontology |
Molecular function |
• chemokine activity
• protein binding
• endopeptidase inhibitor activity
• receptor binding
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Cellular component |
• extracellular region
• extracellular exosome
• membrane attack complex
• extracellular space
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Biological process |
• G-protein coupled receptor signaling pathway
• cytolysis
• complement activation, alternative pathway
• immune system process
• positive regulation of chemokine secretion
• complement activation
• response to stress
• in utero embryonic development
• positive regulation of angiogenesis
• chemotaxis
• cell surface receptor signaling pathway
• activation of MAPK activity
• complement activation, classical pathway
• positive regulation of vascular endothelial growth factor production
• inflammatory response
• regulation of complement activation
• negative regulation of macrophage chemotaxis
• negative regulation of endopeptidase activity
• innate immune response
• cell chemotaxis
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Sources:Amigo / QuickGO |
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Orthologs |
Species |
Human |
Mouse |
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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NM_001735
NM_001317163
NM_001317164
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RefSeq (protein) |
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NP_001304092
NP_001304093
NP_001726
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Location (UCSC) |
Chr 9: 120.95 – 121.05 Mb |
Chr 9: 34.98 – 35.06 Mb |
PubMed search |
[3] |
[4] |
Wikidata |
View/Edit Human |
View/Edit Mouse |
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Complement component 5 is a protein that in humans is encoded by the C5 gene.[5]
Complement component 5 is involved in the complement system. It is cleaved into C5a and C5b:
- C5a plays an important role in chemotaxis.[6]
- C5b forms the first part of the complement membrane attack complex.
Deficiency is thought to cause Leiner's disease.
Contents
- 1 Function
- 2 Clinical significance
- 3 Therapeutic applications
- 4 Complement system pathway
- 5 References
- 6 Further reading
- 7 External links
Function
Complement component 5 is the fifth component of complement, which plays an important role in inflammatory and cell killing processes. This protein is composed of alpha and beta polypeptide chains that are linked by a disulfide bridge. An activation peptide, C5a, which is an anaphylatoxin that possesses potent spasmogenic and chemotactic activity, is derived from the alpha polypeptide via cleavage with a C5-convertase. The C5b macromolecular cleavage product can form a complex with the C6 complement component, and this complex is the basis for formation of the membrane attack complex, which includes additional complement components.[5]
Clinical significance
Mutations in this gene cause complement component 5 deficiency, a disease where patients show a propensity for severe recurrent infections. Defects in this gene have also been linked to a susceptibility to liver fibrosis and to rheumatoid arthritis.[5]
Therapeutic applications
The drug eculizumab (trade name Soliris) prevents cleavage of C5 into C5a and C5b.[7]
Complement system pathway
Membrane attack complex. Some labels are in Polish.
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000106804 - Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026874 - Ensembl, May 2017
- ^ "Human PubMed Reference:".
- ^ "Mouse PubMed Reference:".
- ^ a b c "Entrez Gene: complement component 5".
- ^ Immunology at MCG 1/phagocyt
- ^ Dubois E, Cohen A (2009). "Eculizumab". Br J Clin Pharmacol. 68 (3): 318–319. doi:10.1111/j.1365-2125.2009.03491.x. PMC 2766470 . PMID 19740388.
Further reading
- Tack BF, Morris SC, Prahl JW (1979). "Fifth component of human complement: purification from plasma and polypeptide chain structure". Biochemistry. 18 (8): 1490–7. doi:10.1021/bi00575a016. PMID 106884.
- Fernandez HN, Hugli TE (1978). "Primary structural analysis of the polypeptide portion of human C5a anaphylatoxin. Polypeptide sequence determination and assignment of the oligosaccharide attachment site in C5a". J. Biol. Chem. 253 (19): 6955–64. PMID 690134.
- DiScipio RG (1992). "Formation and structure of the C5b-7 complex of the lytic pathway of complement". J. Biol. Chem. 267 (24): 17087–94. PMID 1387399.
- Haviland DL, Haviland JC, Fleischer DT, et al. (1991). "Complete cDNA sequence of human complement pro-C5. Evidence of truncated transcripts derived from a single copy gene". J. Immunol. 146 (1): 362–8. PMID 1984448.
- Bohnsack JF, Mollison KW, Buko AM, et al. (1991). "Group B streptococci inactivate complement component C5a by enzymic cleavage at the C-terminus". Biochem. J. 273 (Pt 3): 635–40. PMC 1149811 . PMID 1996961.
- Lundwall AB, Wetsel RA, Kristensen T, et al. (1985). "Isolation and sequence analysis of a cDNA clone encoding the fifth complement component". J. Biol. Chem. 260 (4): 2108–12. PMID 2579066.
- Zuiderweg ER, Fesik SW (1989). "Heteronuclear three-dimensional NMR spectroscopy of the inflammatory protein C5a". Biochemistry. 28 (6): 2387–91. doi:10.1021/bi00432a008. PMID 2730871.
- Zuiderweg ER, Nettesheim DG, Mollison KW, Carter GW (1989). "Tertiary structure of human complement component C5a in solution from nuclear magnetic resonance data". Biochemistry. 28 (1): 172–85. doi:10.1021/bi00427a025. PMID 2784981.
- Haefliger JA, Tschopp J, Vial N, Jenne DE (1989). "Complete primary structure and functional characterization of the sixth component of the human complement system. Identification of the C5b-binding domain in complement C6". J. Biol. Chem. 264 (30): 18041–51. PMID 2808363.
- Wetsel RA, Lemons RS, Le Beau MM, et al. (1988). "Molecular analysis of human complement component C5: localization of the structural gene to chromosome 9". Biochemistry. 27 (5): 1474–82. doi:10.1021/bi00405a012. PMID 3365401.
- Zuiderweg ER, Mollison KW, Henkin J, Carter GW (1988). "Sequence-specific assignments in the 1H NMR spectrum of the human inflammatory protein C5a". Biochemistry. 27 (10): 3568–80. doi:10.1021/bi00410a007. PMID 3408713.
- Stewart JL, Kolb WP, Sodetz JM (1987). "Evidence that C5b recognizes and mediates C8 incorporation into the cytolytic complex of complement". J. Immunol. 139 (6): 1960–4. PMID 3624872.
- Buhl AM, Osawa S, Johnson GL (1995). "Mitogen-activated protein kinase activation requires two signal inputs from the human anaphylatoxin C5a receptor". J. Biol. Chem. 270 (34): 19828–32. doi:10.1074/jbc.270.34.19828. PMID 7649993.
- Babkina IN, Seregin SV, Daniliuk NK, et al. (1995). "[Chemico-enzymatic synthesis, cloning and expression of a gene for an analog of human anaphylatoxin C5a]". Bioorg. Khim. 21 (5): 359–64. PMID 7661861.
- Wang X, Fleischer DT, Whitehead WT, et al. (1995). "Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families". J. Immunol. 154 (10): 5464–71. PMID 7730648.
- Oppermann M, Götze O (1995). "Plasma clearance of the human C5a anaphylatoxin by binding to leucocyte C5a receptors". Immunology. 82 (4): 516–21. PMC 1414921 . PMID 7835913.
- Süsal C, Kirschfink M, Kröpelin M, et al. (1994). "Complement activation by recombinant HIV-1 glycoprotein gp120". J. Immunol. 152 (12): 6028–34. PMID 7911492.
- Arribas J, Arizti P, Castaño JG (1994). "Antibodies against the C2 COOH-terminal region discriminate the active and latent forms of the multicatalytic proteinase complex". J. Biol. Chem. 269 (17): 12858–64. PMID 8175701.
- Süsal C, Kirschfink M, Kröpelin M, et al. (1996). "Identification of complement activation sites in human immunodeficiency virus type-1 glycoprotein gp120". Blood. 87 (6): 2329–36. PMID 8630395.
- Ames RS, Li Y, Sarau HM, et al. (1996). "Molecular cloning and characterization of the human anaphylatoxin C3a receptor". J. Biol. Chem. 271 (34): 20231–4. doi:10.1074/jbc.271.34.20231. PMID 8702752.
- Fredslund F, Laursen NS, Roversi P, et al. (2008). "Structure of and influence of a tick complement inhibitor on human complement component 5". Nat Immunol. 9 (7): 753–60. doi:10.1038/ni.1625. PMID 18536718.
External links
- Complement 5 at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
PDB gallery
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1cfa: SOLUTION STRUCTURE OF A SEMI-SYNTHETIC C5A RECEPTOR ANTAGONIST AT PH 5.2, 303K, NMR, 20 STRUCTURES
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1kjs: NMR SOLUTION STRUCTURE OF C5A AT PH 5.2, 303K, 20 STRUCTURES
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1xwe: NMR Structure of C345C (NTR) domain of C5 of complement
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Proteins: complement system (C, L, A)
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Activators/enzymes |
Early |
- A: Factor B
- Factor D
- Factor P/Properdin
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Middle |
- C3-convertase
- C5-convertase
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Late |
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Inhibitors |
- CLA: C1-inhibitor
- Decay-accelerating factor/CD59
- Factor I
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Complement receptors |
- CR1
- CR2
- CR3
- CR4
- CD11b/CD11c/CD18
- Anaphylatoxin
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UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 補体系の概要および臨床的評価 overview and clinical assessment of the complement system
- 2. 補体系の遺伝性疾患 inherited disorders of the complement system
- 3. 補体経路 complement pathways
- 4. 感染症を繰り返す小児に対するアプローチ approach to the child with recurrent infections
- 5. 補体系の後天性欠損 acquired deficiencies of the complement system
English Journal
- Anti-complementary activity of two homogeneous polysaccharides from Eclipta prostrata.
- Wang H1, Li N1, Zhu C1, Shi S1, Jin H2, Wang S3.
- Biochemical and biophysical research communications.Biochem Biophys Res Commun.2017 Nov 18;493(2):887-893. doi: 10.1016/j.bbrc.2017.09.126. Epub 2017 Sep 23.
- PMID 28951216
- The role of complement in the acute phase response after burns.
- Korkmaz HI1, Krijnen PAJ2, Ulrich MMW3, de Jong E4, van Zuijlen PPM5, Niessen HWM6.
- Burns : journal of the International Society for Burn Injuries.Burns.2017 Nov;43(7):1390-1399. doi: 10.1016/j.burns.2017.03.007. Epub 2017 Apr 12.
- PMID 28410933
- Magnetic bead based assays for complement component C5.
- DiScipio RG1, Schraufstatter IU2.
- Journal of immunological methods.J Immunol Methods.2017 Nov;450:50-57. doi: 10.1016/j.jim.2017.07.010. Epub 2017 Jul 27.
- PMID 28757372
Japanese Journal
- A simple PCR-based method for the rapid genotyping of inherited fifth complement component (C5)-deficient mice
- WANG Qingkai,WANG Na,ZHANG Xin [他]
- Experimental animals 64(3), 261-268, 2015-07
- NAID 40020532451
- A simple PCR-based method for the rapid genotyping of inherited fifth complement component (C5)-deficient mice
- WANG Qingkai,WANG Na,ZHANG Xin,HU Weiguo
- Experimental Animals 64(3), 261-268, 2015
- … The fifth component of complement (C5) is considered to be the center of complement activation and function. … Using ARMS-PCR method, we generated C5-deficient mice in the C57BL/6 background over 9 backcrossed generations and further verified the phenotype using complement-mediated hemolytic assays. …
- NAID 130005091026
- 生分解性ポリエステル多孔質膜に支持された培養細胞シート
- 民部 裕洋,田中 孝明
- 膜 40(3), 124-129, 2015
- … Established osteoblast–like (Saos–2) cells grew on a flexible microporous membrane of PCL and hydroxyapatite, the latter of which is a major mineral component of bone and used in bone defect treatment, although the cells grew in a single layer. … The biodegradable microporous sheets including those described in the review will complement the existing cultured cell sheet technology. …
- NAID 130005075555
Related Links
- Covered on Genetics Home Reference: rheumatoid arthritis From NCBI Gene: Eculizumab, poor response to Leiner disease From UniProt: Complement component 5 deficiency (C5D): A rare defect of the complement ...
- [ Complement component 5 ] の検索結果 Complement component 5 From Wikipedia, the free encyclopedia Jump to: navigation, search C5 Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1CFA, 1KJS ...
★リンクテーブル★
[★]
- 英
- complement 5, complement component 5
- 同
- 補体第五成分 fifth component of complement
- 関
- 補体
[★]
- 補って完全にする物、補完物。(免疫)補体
- (必要な)全数、善良
[★]
- 関
- building block、composition、constituent、element、ingredient、moiety