Single point mutations in domain II of the yeast mitochondrial release factor mRF-1 affect ribosome binding (Q27939413)

1

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M Rep

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H J Dubbink

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L A Grivell

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language of work or name

English

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publication date

25 November 1993

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published in

Nucleic Acids Research

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1 December 2016

21

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issue

23

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page(s)

5308-15

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cites work

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The yeast nuclear gene MRF1 encodes a mitochondrial peptide chain release factor and cures several mitochondrial RNA splicing defects

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Selection of lys2 Mutants of the Yeast SACCHAROMYCES CEREVISIAE by the Utilization of alpha-AMINOADIPATE.

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Sequence comparison of new prokaryotic and mitochondrial members of the polypeptide chain release factor family predicts a five-domain model for release factor structure

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Construction of LYS2 cartridges for use in genetic manipulations of Saccharomyces cerevisiae.

2 June 2018

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Influence of codon context on UGA suppression and readthrough

2 June 2018

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2 June 2018

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Localization of the release factor-2 binding site on 70 S ribosomes by immuno-electron microscopy.

2 June 2018

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The ribosomal binding domain for the bacterial release factors RF-1, RF-2 and RF-3

20 June 2018

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12 December 2020

Recognition of termination codon by release factor in the presence of a tRNA-occupied A site. Evidence for flexibility in accommodation of the release factor on the ribosome

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A general method for polyethylene-glycol-induced genetic transformation of bacteria and yeast

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The identification of 18 nuclear genes required for the expression of the yeast mitochondrial gene encoding cytochrome c oxidase subunit 1

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Interaction of the release factor with the Escherichia coli ribosome: inhibition of the 30S subunit domain by specific antibodies

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Epitope-tagging vectors designed for yeast

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Tightly controlled expression systems for the production and purification of Escherichia coli release factor 1

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Ethidium bromide induced mutation of yeast mitochondria: complete transformation of cells into respiratory deficient non-chromosomal "petites"

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