Literature DB >> 6238949

Plasminogens Tochigi II and Nagoya: two additional molecular defects with Ala-600----Thr replacement found in plasmin light chain variants.

T Miyata, S Iwanaga, Y Sakata, N Aoki, J Takamatsu, T Kamiya.   

Abstract

Previous studies in our laboratories (Miyata, T., et al. (1982) Proc. Natl. Acad. Sci. U.S. 79, 6132-6136) showed that the structural defect in a hereditarily abnormal plasminogen, plasminogen Tochigi, is due to replacement of Ala by Thr at position 600 from the NH2-terminal end. In the present studies, two abnormal plasminogens, plasminogens Tochigi II and Nagoya, obtained from other family members were analyzed to identify the structural impairment in these molecules. Amino acid sequence analysis of one of the tryptic peptides isolated, respectively, from plasminogens Tochigi II and Nagoya indicated that in both cases, Ala-600 (equivalent to Ala-55 of the chymotrypsin numbering system) had been replaced by Thr. No other substitutions at the active site and substrate-binding site residues, namely, His-57, Asp-102, Ser-195, and Asp-189, were found in the plasmin light chain variants, indicating that all these residues are intact. Moreover, the NH2-terminal heptapeptide sequences of the plasmin light chain variants isolated from plasminogens Tochigi II and Nagoya were identical to the sequence determined for the normal control. These results indicate that the absence of proteolytic activity of both abnormal molecules is due to the same amino acid substitution as that of previously reported plasminogen Tochigi.

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Year:  1984        PMID: 6238949     DOI: 10.1093/oxfordjournals.jbchem.a134836

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  5 in total

1.  Plasminogen with type-I mutation is polymorphic in the Japanese population.

Authors:  S Kikuchi; Y Yamanouchi; L Li; K Kobayashi; H Ijima; R Miyazaki; S Tsuchiya; H Hamaguchi
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

2.  Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.

Authors:  A Ichinose; E S Espling; J Takamatsu; H Saito; K Shinmyozu; I Maruyama; T E Petersen; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

3.  Cloning and sequence analysis of cDNA for the luminescent protein aequorin.

Authors:  S Inouye; M Noguchi; Y Sakaki; Y Takagi; T Miyata; S Iwanaga; T Miyata; F I Tsuji
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

Review 4.  Clinical disorders of fibrinolysis: a critical review.

Authors:  R B Francis
Journal:  Blut       Date:  1989-07

5.  Breaching the conformational integrity of the catalytic triad of the serine protease plasmin: localized disruption of a side chain of His-603 strongly inhibits the amidolytic activity of human plasmin.

Authors:  A M Mhashilkar; T Viswanatha; B A Chibber; F J Castellino
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-01       Impact factor: 11.205

  5 in total

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