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PMID: 6257674 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification of the active amino acid residue of the polypeptide of ATP-dependent protein breakdown.

The Journal of biological chemistry ·Vol. 256 ·No. 4 ·1981-02-25 ·Pages 1525-8

Hershko A, Ciechanover A, Rose IA

Abstract

The heat-stable polypeptide of the ATP-dependent proteolytic system was previously found to form covalent conjugates with proteins and to be activated by ATP in an adenylylation mechanism. To identify the functional amino acid of the polypeptide, the activated residue was specifically labeled by the reductive cleavage of the intermediate with [3H]borohydride. Following acid hydrolysis, the reduced labeled derivative was found to be completely oxidizable by periodate with formation of [3H]formaldehyde, and was identified as ethanolamine by thin layer chromatography, electrophoresis, and amino acid analyzer chromatography. These results indicate that the activated amino acid residue of the polypeptide is COOH-terminal glycine.

MeSH Terms
Adenosine Triphosphate Amino Acids/analysis Animals Borohydrides Chromosomal Proteins, Non-Histone/blood Erythrocytes/analysis Glycine/analysis Humans Rabbits Reticulocytes/enzymology Tritium Ubiquitins
Chemicals
Amino Acids Borohydrides Chromosomal Proteins, Non-Histone Ubiquitins Tritium Adenosine Triphosphate Glycine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hershko A
Ciechanover A
Rose I A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1981-02-25
Pages
1525-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIADDK NIH HHS · AM-25614-01 · United States
NCI NIH HHS · CA-06927 · United States
NCRR NIH HHS · RR-05539 · United States
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