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Initiation of mRNA translation in prokaryotes

Biochemistry (Easton), 1990-06, Vol.29 (25), p.5881-5889

1990

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Identification of a Cold Shock Transcriptional Enhancer of the Escherichia coli Gene Encoding Nucleoid Protein H-NS

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (23), p.10907-10911

1991

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Initiation factors in the early events of mRNA translation in bacteria

Cold Spring Harbor Symposia on Quantitative Biology, 2001, Vol.66, p.363-376

2001

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Translation of mRNAs With Degenerate Initiation Triplet AUU Displays High Initiation Factor 2 Dependence and is Subject to Initiation Factor 3 Repression

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (9), p.4161-4165

1993

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Selection of the mRNA Translation Initiation Region by Escherichia coli Ribosomes

Proceedings of the National Academy of Sciences - PNAS, 1988-09, Vol.85 (17), p.6427-6431

1988

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Translation initiation factor IF3: two domains, five functions, one mechanism?

The EMBO journal, 2001-08, Vol.20 (16), p.4560-4569

2001

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Massive presence of the Escherichia coli 'major cold-shock protein' CspA under non-stress conditions

The EMBO journal, 1999-03, Vol.18 (6), p.1653-1659

1999

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Mutagenesis of the downstream region of the Escherichia coli hns promoter

Biochimie, 2001-02, Vol.83 (2), p.251-259

2001

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Interaction of the main cold shock protein CS7.4 (CspA) of Escherichia coli with the promoter region of hns

Biochimie, 1994, Vol.76 (10), p.1090-1098

1994

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Molecular dissection of translation initiation factor IF2. Evidence for two structural and functional domains

The Journal of biological chemistry, 1991-09, Vol.266 (25), p.16356-16362

1991

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The oligomeric structure of nucleoid protein H-NS is necessary for recognition of intrinsically curved DNA and for DNA bending

The EMBO journal, 1997-04, Vol.16 (7), p.1795-1805

1997

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Post‐transcriptional regulation of CspA expression in Escherichia coli

Molecular microbiology, 1996-01, Vol.19 (2), p.231-240

1996

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Mapping the fMet-tRNA(f)(Met) binding site of initiation factor IF2

The EMBO journal, 2000-10, Vol.19 (19), p.5233

2000

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Proteins from the prokaryotic nucleoid: primary and quaternary structure of the 15‐kD Escherichia coli DNA binding protein H‐NS

Molecular microbiology, 1988-05, Vol.2 (3), p.323-329

1988

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The C-terminal Subdomain (IF2 C-2) Contains the Entire fMet-tRNA Binding Site of Initiation Factor IF2

The Journal of biological chemistry, 2000-01, Vol.275 (4), p.2447-2454

2000

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Multimeric self-assembly equilibria involving the histone-like protein H-NS. A thermodynamic study

The Journal of biological chemistry, 2000-01, Vol.275 (2), p.729-734

2000

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Ribosome-independent GTPase activity of translation initiation factor IF2 and of its G-domain

The Journal of biological chemistry, 1991-12, Vol.266 (34), p.22800-22802

1991

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Proteins from the prokaryotic nucleoid Interaction of nucleic acids with the 15 kDa Escherichia coli histone-like protein H-NS

FEBS letters, 1988-02, Vol.229 (1), p.197-202

1988

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Structure-function relationship in Escherichia coli initiation factors. Biochemical and biophysical characterization of the interaction between IF-2 and guanosine nucleotides

The Journal of biological chemistry, 1985-07, Vol.260 (15), p.8918-8924

1985

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Escherichia coli DNA-binding protein H-NS is localized in the nucleoid

Research in microbiology, 1991, Vol.142 (4), p.373-380

1991

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Antagonistic involvement of FIS and H‐NS proteins in the transcriptional control of hns expression

Molecular microbiology, 1996-03, Vol.19 (5), p.965-975

1996

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Translation during cold adaptation does not involve mRNA–rRNA base pairing through the downstream box

RNA (Cambridge), 2000-10, Vol.6 (10), p.1393-1402, Article S1355838200000595

2000

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Transcriptional and Post-transcriptional Control of Cold-shock Genes

Journal of molecular biology, 2003-08, Vol.331 (3), p.527-539

2003

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Expression of the gene encoding the major bacterial nucleoid protein H‐NS is subject to transcriptional auto‐repression

Molecular microbiology, 1993-10, Vol.10 (2), p.273-282

1993

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Site-directed mutagenesis and NMR spectroscopic approaches to the elucidation of the structure-function relationships in translation initiation factors IF1 and IF3

Biochimie, 1991-07, Vol.73 (7), p.1001-1006

1991

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Initiation of mRNA translation in prokaryotes

Identification of a Cold Shock Transcriptional Enhancer of the Escherichia coli Gene Encoding Nucleoid Protein H-NS

Initiation factors in the early events of mRNA translation in bacteria

Translation of mRNAs With Degenerate Initiation Triplet AUU Displays High Initiation Factor 2 Dependence and is Subject to Initiation Factor 3 Repression

Selection of the mRNA Translation Initiation Region by Escherichia coli Ribosomes

Translation initiation factor IF3: two domains, five functions, one mechanism?

Massive presence of the Escherichia coli 'major cold-shock protein' CspA under non-stress conditions

Mutagenesis of the downstream region of the Escherichia coli hns promoter

Interaction of the main cold shock protein CS7.4 (CspA) of Escherichia coli with the promoter region of hns

Molecular dissection of translation initiation factor IF2. Evidence for two structural and functional domains

The oligomeric structure of nucleoid protein H-NS is necessary for recognition of intrinsically curved DNA and for DNA bending

Post‐transcriptional regulation of CspA expression in Escherichia coli

Mapping the fMet-tRNA(f)(Met) binding site of initiation factor IF2

Proteins from the prokaryotic nucleoid: primary and quaternary structure of the 15‐kD Escherichia coli DNA binding protein H‐NS

The C-terminal Subdomain (IF2 C-2) Contains the Entire fMet-tRNA Binding Site of Initiation Factor IF2

Multimeric self-assembly equilibria involving the histone-like protein H-NS. A thermodynamic study

Ribosome-independent GTPase activity of translation initiation factor IF2 and of its G-domain

Proteins from the prokaryotic nucleoid Interaction of nucleic acids with the 15 kDa Escherichia coli histone-like protein H-NS

Structure-function relationship in Escherichia coli initiation factors. Biochemical and biophysical characterization of the interaction between IF-2 and guanosine nucleotides

Escherichia coli DNA-binding protein H-NS is localized in the nucleoid

Antagonistic involvement of FIS and H‐NS proteins in the transcriptional control of hns expression

Translation during cold adaptation does not involve mRNA–rRNA base pairing through the downstream box

Transcriptional and Post-transcriptional Control of Cold-shock Genes

Expression of the gene encoding the major bacterial nucleoid protein H‐NS is subject to transcriptional auto‐repression

Site-directed mutagenesis and NMR spectroscopic approaches to the elucidation of the structure-function relationships in translation initiation factors IF1 and IF3

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