Zobrazeno 1 - 3
of 3
pro vyhledávání: '"D. B. Ault-Riche"'
Publikováno v:
Archives of Biochemistry and Biophysics. 319:365-371
S -Adenosylhomocysteine (AdoHcy) hydrolase was subjected to limited proteolytic digestion utilizing the proteases trypsin, V8, and papain. Results of the trypsin digest revealed one major susceptible peptide bond between amino acid residues 103 and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8358e1a64aa07003f38a0e42973da9e1
https://doi.org/10.1006/abbi.1995.1306
https://doi.org/10.1006/abbi.1995.1306
Autor:
Michael S. Wolfe, David R. Borcherding, Ronald T. Borchardt, H. Liang, D. B. Ault-Riche, M. Hasobe
Publikováno v:
Antiviral Chemistry and Chemotherapy. 4:245-248
Two synthetic analogues of aristeromycin, which were shown in a separate study to be inhibitors of S-adenosylhomocysteine hydrolase and devoid of substrate activity with adenosine kinase and adenosine deaminase, were found in this study to inhibit va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea1ab9ed662b3b580d7628bcaddefa2d
https://doi.org/10.1177/095632029300400408
https://doi.org/10.1177/095632029300400408
Publikováno v:
Antiviral Chemistry and Chemotherapy. 4:127-130
(1′R,2′S,3′R)-9-(2′,3′-Dihydroxycycloperrt-4′-en-1′-yl)-adenine (DHCeA) and -3-deazaadenine (3-deaza-DHCeA), which are potent inhibitors of S-adenosylho-mocysteine (AdoHcy) hydrolase, and ribavirin, which is an inhibitor of IMP-dehydrog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7beb41cd883124b66bef268cf2dc2a65
https://doi.org/10.1177/095632029300400207
https://doi.org/10.1177/095632029300400207