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Paper3036070

Complete amino acid sequence of the A chain of human complement-classical-pathway enzyme C1r.

Arlaud GJ and 2 others. Biochem J, 1987. Cited by 51 papers, by iCite.

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ConductScience Library. Complete amino acid sequence of the A chain of human complement-classical-pathway enzyme C1r. Papers, record 3036070. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/3036070

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Complete amino acid sequence of the A chain of human complement-classical-pathway enzyme C1r.
PubMed
Journal
Biochem J
PubMed
Year
1987
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
51
iCite
Relative citation ratio, by iCite
1.35
iCite
Revised in PubMed
2019-05-01
PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Arlaud GJG J
2Willis ACA C
3Gagnon JJ

Source PubMed

Topics7

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Complement Activating EnzymesMajor topic
Complement C1Major topic
Amino Acid Sequence
Amino Acids
Complement C1r
Humans
Peptide Fragments

Source PubMed

References28

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
1869,924The structure and enzymic activities of the C1r and C1s subcomponents of C1, the first component of human serum complement.Biochem J1977https://conductscience.org/library/papers/869924PubMed
213,753,215beta-Hydroxyaspartic acid: synthesis and separation of its diastereoisomers.Arch Biochem Biophys1960https://conductscience.org/library/papers/13753215PubMed
340,870Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents.Mol Immunol1979https://conductscience.org/library/papers/40870PubMed
46,250,896Calcium binding properties of the C1 subcomponents C1q, C1r and C1s.FEBS Lett1980https://conductscience.org/library/papers/6250896PubMed
56,254,570Purified proenzyme C1r. Some characteristics of its activation and subsequent proteolytic cleavage.Biochim Biophys Acta1980https://conductscience.org/library/papers/6254570PubMed
67,023,363The proteolytic activation systems of complement.Annu Rev Biochem1981https://conductscience.org/library/papers/7023363PubMed
76,281,620The human complement system serine proteases C1r and C1s and their proenzymes.Methods Enzymol1981https://conductscience.org/library/papers/6281620PubMed
86,282,261The catalytic chain of human complement subcomponent C1r. Purification and N-terminal amino acid sequences of the major cyanogen bromide-cleavage fragments.Biochem J1982https://conductscience.org/library/papers/6282261PubMed
97,092,811
Isolation, characterization and N-terminal sequences of the CNBr-cleavage peptides from human complement Factor B. Localization of a free thiol group and a sequence defining the site cleaved by factor D.
Biochem J1982https://conductscience.org/library/papers/7092811PubMed
106,572,939beta-Hydroxyaspartic acid in vitamin K-dependent protein C.Proc Natl Acad Sci U S A1983https://conductscience.org/library/papers/6572939PubMed
116,303,394Complete amino acid sequence of the catalytic chain of human complement subcomponent C1-r.Biochemistry1983https://conductscience.org/library/papers/6303394PubMed
126,871,167Complete amino acid sequence of the light chain of human blood coagulation factor X: evidence for identification of residue 63 as beta-hydroxyaspartic acid.Biochemistry1983https://conductscience.org/library/papers/6871167PubMed
136,688,526The occurrence of beta-hydroxyaspartic acid in the vitamin K-dependent blood coagulation zymogens.Biochem Biophys Res Commun1983https://conductscience.org/library/papers/6688526PubMed
146,630,196Beta-hydroxyaspartic acid in vitamin K-dependent proteins.J Biol Chem1983https://conductscience.org/library/papers/6630196PubMed
156,692,907erythro-beta-Hydroxyaspartic acid in bovine factor IX and factor X.FEBS Lett1984https://conductscience.org/library/papers/6692907PubMed
166,425,296Derivatives of blood coagulation factor IX contain a high affinity Ca2+-binding site that lacks gamma-carboxyglutamic acid.J Biol Chem1984https://conductscience.org/library/papers/6425296PubMed
176,546,930Calcium-binding properties of bovine factor X lacking the gamma-carboxyglutamic acid-containing region.J Biol Chem1984https://conductscience.org/library/papers/6546930PubMed
186,329,734The gene structure of human anti-haemophilic factor IX.EMBO J1984https://conductscience.org/library/papers/6329734PubMed
196,091,100Cloning and sequencing of liver cDNA coding for bovine protein C.Proc Natl Acad Sci U S A1984https://conductscience.org/library/papers/6091100PubMed
206,149,573Activation of C1.Philos Trans R Soc Lond B Biol Sci1984https://conductscience.org/library/papers/6149573PubMed

See all 28 references

Cited by10

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 51 citations.

PMIDTitleJournalYearIn PapersSource
31,749,804C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome.Front Immunol2019https://conductscience.org/library/papers/31749804PubMed
15,527,420A novel human complement-related protein, C1r-like protease (C1r-LP), specifically cleaves pro-C1s.Biochem J2005https://conductscience.org/library/papers/15527420PubMed
11,823,416The crystal structure of the zymogen catalytic domain of complement protease C1r reveals that a disruptive mechanical stress is required to trigger activation of the C1 complex.EMBO J2002https://conductscience.org/library/papers/11823416PubMed
8,136,028Chemical characterization and location of ionic interactions involved in the assembly of the C1 complex of human complement.J Protein Chem1993https://conductscience.org/library/papers/8136028PubMed
3,262,057The role of beta-hydroxyaspartate and adjacent carboxylate residues in the first EGF domain of human factor IX.EMBO J1988https://conductscience.org/library/papers/3262057PubMed
2,954,545Characterization of primary amino acid sequence of human complement control protein factor I from an analysis of cDNA clones.Biochem J1987https://conductscience.org/library/papers/2954545PubMed
2,825,166Occurrence of beta-hydroxylated asparagine residues in non-vitamin K-dependent proteins containing epidermal growth factor-like domains.Proc Natl Acad Sci U S A1987https://conductscience.org/library/papers/2825166PubMed
2,556,995The quaternary structure in solution of human complement subcomponent C1r2C1s2.Biochem J1989https://conductscience.org/library/papers/2556995PubMed
2,539,098Isolation and functional characterization of the proenzyme form of the catalytic domains of human C1r.Biochem J1989https://conductscience.org/library/papers/2539098PubMed
2,535,773Genetic studies of low-abundance human plasma proteins. XIII. Population genetics of C1R complement subcomponent and description of new variants.Am J Hum Genet1989https://conductscience.org/library/papers/2535773PubMed

Genes3

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
C1R715Swiss-Prot's referenceshttps://conductscience.org/library/genes/715NCBI Gene
F92,158PubTator's text mininghttps://conductscience.org/library/genes/2158NCBI Gene
PROC5,624PubTator's text mininghttps://conductscience.org/library/genes/5624NCBI Gene

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

None in this release

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  • Comments and corrections
  • Drugs
  • Data

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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