MolPharm

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by ScaronKODA, J.
Right arrow Articles by ScaronORM, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by ScaronKODA, J.
Right arrow Articles by ScaronORM, F.

Molecular Pharmacology, Vol 2, 608-610, Copyright © 1966 by the American Society for Pharmacology and Experimental Therapeutics

Formation of a Dead Code Triplet through Replacement of the Terminal Ribonucleoside in Guanylyl-Uridylyl-Uridine and Guanylyl-Uridylyl-Cytidine by 6-Azacytidine

J. ScaronKODA 1, V. LISYacute 1, J. SMRT 1, A. HOLYacute 1, and F. ScaronORM 1

1 Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, Prague, Czechoslovakia

The binding of valyl-tRNA to ribosomes in vitro, stimulated by guanylyl-uridylyluridine and guanylyl-uridylyl-cytidine is not effected by guanylyl-uridylyl-6-azacytidine. This finding indicates the high chemical specificity of the pyrimidine components of the codon.

Note:
We express our thanks to the workers of the Isotope Laboratory of this Institute for radioactivity counts.

Submitted on September 30, 1966







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1966 by the American Society for Pharmacology and Experimental Therapeutics