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PMID: 6092377 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

RNA capping by the vaccinia virus guanylyltransferase. Structure of enzyme-guanylate intermediate.

The Journal of biological chemistry ·Vol. 259 ·No. 21 ·1984-11-10 ·Pages 13488-94

Roth MJ, Hurwitz J

Abstract

GTP:RNA guanylyltransferase isolated from vaccinia virus catalyzes the transfer of GMP from GTP to the 5' terminus of RNA via an enzyme-guanylate intermediate. Incubation of the purified vaccinia RNA guanylyltransferase with [alpha- 32P]GTP and MgCl2 yields [32P]GMP covalently linked to the Mr = 95,000 subunit. The bond involves the phosphate moiety of GMP and the Ne-amino group of lysine. This was verified by treatment of the isolated 95-kDa subunit-[32P]GMP complex with sodium periodate, followed by methylamine-catalyzed beta-elimination. The product was then hydrolyzed by alkali producing 32P-labeled lysine (Ne-P)phosphate.

MeSH Terms
Endopeptidases Guanosine Triphosphate/metabolism HeLa Cells/enzymology Humans Molecular Weight Nucleotidyltransferases/isolation & purification,metabolism Peptide Fragments/analysis Protein Binding RNA Caps/metabolism Vaccinia virus/enzymology
Chemicals
Peptide Fragments RNA Caps Guanosine Triphosphate Nucleotidyltransferases guanylyltransferase Endopeptidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Roth M J
Hurwitz J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1984-11-10
Pages
13488-94
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GMO 749-07 · United States
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