Paper7092811
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.
Christie DL and 1 other. Biochem J, 1982. Cited by 35 papers, by iCite.
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ConductScience Library. 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. Papers, record 7092811. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7092811
Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
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.
- PubMed
Topics10
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Complement Activating Enzymes | Major topic |
| Peptide Fragments | Major topic |
| Amino Acid Sequence | |
| Amino Acids | |
| Amino Sugars | |
| Chromatography, Gel | |
| Chromatography, High Pressure Liquid | |
| Cyanogen Bromide | |
| Humans | |
| Sulfhydryl Compounds |
Source PubMed
References26
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 1,227,961 | The quantitation of glucosamine and galactosamine in glycoproteins after hydrolysis in p-toluenesulphonic acid. | FEBS Lett | 1975 | https://conductscience.org/library/papers/1227961 | PubMed |
| 2 | 5,432,063 | Cleavage of structural proteins during the assembly of the head of bacteriophage T4. | Nature | 1970 | https://conductscience.org/library/papers/5432063 | PubMed |
| 3 | 458,145 | The alternative pathway C3/C5 convertase: chemical basis of factor B activation. | J Immunol | 1979 | https://conductscience.org/library/papers/458145 | PubMed |
| 4 | 786,150 | Comparative aspects of glycoprotein structure. | Annu Rev Biochem | 1976 | https://conductscience.org/library/papers/786150 | PubMed |
| 5 | 6,997,298 | Structural evidence that complement factor B constitutes a novel class of serine protease. | J Biol Chem | 1980 | https://conductscience.org/library/papers/6997298 | PubMed |
| 6 | 261,515 | Limited proteolysis of complement components C2 and factor B. Structural analogy and limited sequence homology. | Biochem J | 1979 | https://conductscience.org/library/papers/261515 | PubMed |
| 7 | 667,015 | Direct microsequence analysis of polypeptides using an improved sequenator, a nonprotein carrier (polybrene), and high pressure liquid chromatography. | Biochemistry | 1978 | https://conductscience.org/library/papers/667015 | PubMed |
| 8 | 1,006,167 | The serine protease nature of the C3 and C5 convertases of the classical and alternative complement pathways. | Scand J Immunol | 1976 | https://conductscience.org/library/papers/1006167 | PubMed |
| 9 | 352,622 | A molecular approach to the complement system. | Curr Top Cell Regul | 1978 | https://conductscience.org/library/papers/352622 | PubMed |
| 10 | 6,769,474 | Amino-terminal sequence of human factor B of the alternative complement pathway and its cleavage fragments, Ba and Bb. | Biochemistry | 1980 | https://conductscience.org/library/papers/6769474 | PubMed |
| 11 | 728,424 | Sequence of the amino-terminal 349 residues of rabbit muscle glycogen phosphorylase including the sites of covalent and allosteric control. | Biochemistry | 1978 | https://conductscience.org/library/papers/728424 | PubMed |
| 12 | 5,093,780 | Functional relationship of factor B in the properdin system to C3 proactivator of human serum. | J Immunol | 1971 | https://conductscience.org/library/papers/5093780 | PubMed |
| 13 | 5,778,667 | An examination of conditions for the cleavage of polypeptide chains with cyanogen bromide: application to catalase. | Arch Biochem Biophys | 1969 | https://conductscience.org/library/papers/5778667 | PubMed |
| 14 | 6,821,372 | Factor D of the alternative pathway of human complement. Purification, alignment and N-terminal amino acid sequences of the major cyanogen bromide fragments, and localization of the serine residue at the active site. | Biochem J | 1980 | https://conductscience.org/library/papers/6821372 | PubMed |
| 16 | 7,258,621 | Use of fluorescamine as an effective blocking reagent to reduce the background in protein sequence analyses by the Beckman automated sequencer. | Anal Biochem | 1981 | https://conductscience.org/library/papers/7258621 | PubMed |
| 17 | 5,499,437 | Isolation and properties of a glycine-rich beta-glycoprotein of human serum. | Biochim Biophys Acta | 1970 | https://conductscience.org/library/papers/5499437 | PubMed |
| 18 | 417,728 | The purification and properties of the second component of human complement. | Biochem J | 1978 | https://conductscience.org/library/papers/417728 | PubMed |
| 19 | 411,505 | Chemical characterization of human factor B of the alternate pathway of complement activation. | Biochemistry | 1977 | https://conductscience.org/library/papers/411505 | PubMed |
| 20 | 488,920 | A cheap and simple method to achieve and maintain the necessary purity of reagents and solvents for automated amino acid sequence determination with the sequenator. | Hoppe Seylers Z Physiol Chem | 1979 | https://conductscience.org/library/papers/488920 | PubMed |
| 21 | 7,023,363 | The proteolytic activation systems of complement. | Annu Rev Biochem | 1981 | https://conductscience.org/library/papers/7023363 | PubMed |
Cited by15
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 35 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 7,103,942 | Purification of human C3b inactivator by monoclonal-antibody affinity chromatography. | Biochem J | 1982 | https://conductscience.org/library/papers/7103942 | PubMed |
| 6,555,044 | 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. | Biochem J | 1983 | https://conductscience.org/library/papers/6555044 | PubMed |
| 6,526,007 | PC13 embryonal carcinoma-derived growth factor. | EMBO J | 1984 | https://conductscience.org/library/papers/6526007 | PubMed |
| 6,342,610 | Amino acid sequence of the Bb fragment from complement Factor B. Sequence of the major cyanogen bromide-cleavage peptide (CB-II) and completion of the sequence of the Bb fragment. | Biochem J | 1983 | https://conductscience.org/library/papers/6342610 | PubMed |
| 6,342,609 | Amino acid sequence of the Bb fragment from human complement Factor B. Alignment of the cyanogen bromide-cleavage peptides. | Biochem J | 1983 | https://conductscience.org/library/papers/6342609 | PubMed |
| 6,323,161 | Internal homologies of the Ba fragment from human complement component Factor B, a class III MHC antigen. | EMBO J | 1984 | https://conductscience.org/library/papers/6323161 | PubMed |
| 3,036,070 | Complete amino acid sequence of the A chain of human complement-classical-pathway enzyme C1r. | Biochem J | 1987 | https://conductscience.org/library/papers/3036070 | PubMed |
| 3,030,276 | Chemical modification of the haem propionate of cytochrome c. A re-evaluation of the reaction of cytochrome c with a water-soluble carbodi-imide. | Biochem J | 1986 | https://conductscience.org/library/papers/3030276 | PubMed |
| 2,983,658 | Primary structure of the A chain of human complement-classical-pathway enzyme C1r. N-terminal sequences and alignment of autolytic fragments and CNBr-cleavage peptides. | Biochem J | 1985 | https://conductscience.org/library/papers/2983658 | PubMed |
| 2,963,625 | The complete amino acid sequence of human complement factor H. | Biochem J | 1988 | https://conductscience.org/library/papers/2963625 | PubMed |
| 2,962,936 | Sequence polymorphism of human complement factor H. | Immunogenetics | 1988 | https://conductscience.org/library/papers/2962936 | PubMed |
| 2,954,816 | The primary structure of the beta-subunit of the cell surface adhesion glycoproteins LFA-1, CR3 and p150,95 and its relationship to the fibronectin receptor. | EMBO J | 1987 | https://conductscience.org/library/papers/2954816 | PubMed |
| 2,951,479 | Human C3b/C4b receptor (CR1). Demonstration of long homologous repeating domains that are composed of the short consensus repeats characteristics of C3/C4 binding proteins. | J Exp Med | 1987 | https://conductscience.org/library/papers/2951479 | PubMed |
| 2,937,401 | CNBr cleavage of the light chain of human complement factor I and alignment of the fragments. | Biochem J | 1986 | https://conductscience.org/library/papers/2937401 | PubMed |
| 2,829,834 | The effects of autolysis on the structure of chicken calpain II. | Biochem J | 1987 | https://conductscience.org/library/papers/2829834 | PubMed |
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The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes |
|---|---|---|---|
| CFB | 629 | PubTator's text mining | https://conductscience.org/library/genes/629 |
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- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
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- 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
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