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PMID: 7729561 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molecular cloning and expression of subunit 12: a non-MCP and non-ATPase subunit of the 26 S protease.

FEBS letters ·Vol. 363 ·No. 1-2 ·1995-04-17 ·Pages 97-100

Dubiel W, Ferrell K, Dumdey R, Standera S, Prehn S, Rechsteiner M

Abstract

A cDNA encoding subunit 12 (S12) of human erythrocyte 26 S protease has been isolated, sequenced and expressed. The cDNA contains an open reading frame that encodes a 36.6 kDA protein 96% identical to mouse Mov-34 and 67% identical to its Drosophila melanogaster homolog. Based on the high degree of sequence identity between human S12, mouse and Drosophila Mov-34 proteins, we conclude that the Mov-34 gene product is a component of the 26 S protease. Antibodies produced against two S12 fragments, Met1-Tyr95 (S12f95) and Met1-Leu205 (S12f205), react with S12 transferred to nitrocellulose from SDS-PAGE. In contrast, after transfer from native gels, the epitope(s) recognized by anti-S12f205 is exposed in the regulatory complex but appears to be masked when the regulatory complex associates with the multicatalytic protease.

MeSH Terms
Amino Acid Sequence Animals Cloning, Molecular DNA, Complementary/chemistry Drosophila melanogaster Erythrocytes/enzymology Gene Expression Humans Immunoblotting Intracellular Signaling Peptides and Proteins Molecular Sequence Data Open Reading Frames Peptide Hydrolases/chemistry,genetics Polymerase Chain Reaction Proteasome Endopeptidase Complex Protein Subunits/chemistry Proteins RNA-Binding Proteins Recombinant Proteins/chemistry Retroviridae Proteins/chemistry Sequence Alignment Sequence Homology
Chemicals
DNA, Complementary Intracellular Signaling Peptides and Proteins PSMD7 protein, human Protein Subunits Proteins RNA-Binding Proteins Recombinant Proteins Retroviridae Proteins Psmd7 protein, mouse Peptide Hydrolases Proteasome Endopeptidase Complex ATP dependent 26S protease
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dubiel W
Institut für Biochemie, Universitätsklinikum Charité, Humboldt-Universität, Berlin, Germany.
Ferrell K
Dumdey R
Standera S
Prehn S
Rechsteiner M
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1995-04-17
Pages
97-100
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NIGMS NIH HHS · GM37009 · United States
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