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PMID: 1281318 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Overproduced rho factor from p39AS has lysine replacing glutamic acid at residue 155 in the linker region between its RNA and ATP binding domains.

Nucleic acids research ·Vol. 20 ·No. 22 ·1992-11-25 ·Pages 6107

Nehrke KW, Seifried SE, Platt T

Abstract

暂无摘要

MeSH Terms
Adenosine Triphosphate/metabolism Binding Sites Cloning, Molecular Glutamates/genetics Glutamic Acid Lysine/genetics Mutation Plasmids RNA/metabolism Rho Factor/genetics,metabolism
Chemicals
Glutamates Rho Factor Glutamic Acid RNA Adenosine Triphosphate Lysine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nehrke K W
Department of Biochemistry, University of Rochester Medical Center, NY 14642.
Seifried S E
Platt T
References (3)
3 references, click to expand
  1. Mutant rho factors with increased transcription termination activities. I. Functional correlations of the primary and secondary polynucleotide binding sites with the efficiency and site-selectivity of rho-dependent termination.
    J Mol Biol. 1989 Nov 5;210(1):23-37 PMID: 2479756
  2. Mutations in an RNP1 consensus sequence of Rho protein reduce RNA binding affinity but facilitate helicase turnover.
    J Biol Chem. 1991 Sep 15;266(26):17296-305 PMID: 1716628
  3. Maximizing gene expression from plasmid vectors containing the lambda PL promoter: strategies for overproducing transcription termination factor rho.
    Proc Natl Acad Sci U S A. 1985 Jan;82(1):88-92 PMID: 3155859
Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1992-11-25
Pages
6107
Language
English
Region
England
NLM ID
0411011
PMCID
PMC334486
Subset
IM
Grants
NIAID NIH HHS · 1T32AI-07362 · United States
NIGMS NIH HHS · 5-RO1-GM35658 · United States
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