Literature DB >> 6303394

Complete amino acid sequence of the catalytic chain of human complement subcomponent C1-r.

G J Arlaud, J Gagnon.   

Abstract

The amino acid sequence of human C1-r b chain hs been determined, from sequence analysis performed on fragments obtained by CNBr cleavage, dilute acid hydrolysis, tryptic cleavage of the succinylated protein, and subcleavages by staphylococcal protease. The polypeptide chain contains 242 amino acids (Mr 27 096), and the sequence shows strong homology with other mammalian serine proteases. The histidine, aspartic acid, and serine residues of the active site (His-57, Asp-102, and Ser-195 in bovine chymotrypsinogen) are located at positions 39, 94, and 191, respectively. The chain which lacks the "histidine-loop" disulfide bridge, contains five half-cystine residues, of which four (positions 157-176 and 187-217) are homologous to residues involved in disulfide bonds generally conserved in serine proteases, whereas the half-cystine residue at position 114 is likely to be involved in the single disulfide bridge connecting the catalytic b chain to the n-terminal a chain. Two carbohydrate moieties are attached to the polypeptide chain, both via asparagine residues at positions 51 and 118.

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Year:  1983        PMID: 6303394     DOI: 10.1021/bi00277a003

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  10 in total

1.  The quaternary structure in solution of human complement subcomponent C1r2C1s2.

Authors:  S J Perkins; A S Nealis
Journal:  Biochem J       Date:  1989-10-15       Impact factor: 3.857

2.  Isolation and functional characterization of the proenzyme form of the catalytic domains of human C1r.

Authors:  M B Lacroix; C A Aude; G J Arlaud; M G Colomb
Journal:  Biochem J       Date:  1989-02-01       Impact factor: 3.857

3.  Genetic studies of low-abundance human plasma proteins. XIII. Population genetics of C1R complement subcomponent and description of new variants.

Authors:  M I Kamboh; L A Lyons; R E Ferrell
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

4.  Cloning and sequencing of full-length cDNA encoding the precursor of human complement component C1r.

Authors:  A Journet; M Tosi
Journal:  Biochem J       Date:  1986-12-15       Impact factor: 3.857

5.  Domain structure and associated functions of subcomponents C1r and C1s of the first component of human complement.

Authors:  C L Villiers; G J Arlaud; M G Colomb
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

6.  Autoactivation of human complement subcomponent C1r involves structural changes reflected in modifications of intrinsic fluorescence, circular dichroism and reactivity with monoclonal antibodies.

Authors:  C L Villiers; G J Arlaud; M G Colomb
Journal:  Biochem J       Date:  1983-11-01       Impact factor: 3.857

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

Authors:  G J Arlaud; A C Willis; J Gagnon
Journal:  Biochem J       Date:  1987-02-01       Impact factor: 3.857

8.  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.

Authors:  J Gagnon; G J Arlaud
Journal:  Biochem J       Date:  1985-01-01       Impact factor: 3.857

9.  The serine proteinase chain of human complement component C1s. Cyanogen bromide cleavage and N-terminal sequences of the fragments.

Authors:  P E Carter; B Dunbar; J E Fothergill
Journal:  Biochem J       Date:  1983-12-01       Impact factor: 3.857

10.  A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism.

Authors:  T C Tsang; D R Bentley; R S Mibashan; F Giannelli
Journal:  EMBO J       Date:  1988-10       Impact factor: 11.598

  10 in total

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