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Literature DB >> 16789252

Phosphorylation of the beta' Subunit of RNA Polymerase and Other Host Proteins upon phiCd1 Infection of Caulobacter crescentus.

Abstract

A protein kinase activity is induced early after infection of Caulobacter crescentus by the DNA phage phiCd1. After phage infection at least 40 proteins are phosphorylated; these include DNA-binding proteins, a membrane-associated protein, and several ribosomal proteins. One of the phosphorylated DNA-binding proteins was identified as the beta' subunit of the host RNA polymerase.

Entities: Species

Year: 1985 PMID： 16789252 PMCID： PMC254920

Source DB: PubMed Journal: J Virol ISSN： 0022-538X Impact factor: 5.103

15 in total

1. BIOLOGICAL PROPERTIES AND CLASSIFICATION OF THE CAULOBACTER GROUP.

Authors: J S POINDEXTER
Journal: Bacteriol Rev Date: 1964-09

2. Caulobacter crescentus RNA polymerase. Purification and characterization of holoenzyme and core polymerase.

Authors: K Amemiya; C W Wu; L Shapiro
Journal: J Biol Chem Date: 1977-06-25 Impact factor: 5.157

3. Control of gene expression in bacteriophage T7: transcriptional controls.

Authors: H Ponta; H J Rahmsdorf; S H Pai; M Hirsch-Kauffmann; P Herrlich; M Schweiger
Journal: Mol Gen Genet Date: 1974

4. Characterization of a protein acyl kinase from Caulobacter crescentus.

Authors: N Agabian; O M Rosen; L Shapiro
Journal: Biochem Biophys Res Commun Date: 1972-12-18 Impact factor: 3.575

5. RNase III is positively regulated by T7 protein kinase.

Authors: J E Mayer; M Schweiger
Journal: J Biol Chem Date: 1983-05-10 Impact factor: 5.157

6. Physical map of Caulobacter crescentus bacteriophage phi Cd1 DNA.

Authors: B Raboy; L Shapiro; K Amemiya
Journal: J Virol Date: 1980-05 Impact factor: 5.103

7. Synthesis of specific membrane proteins is a function of DNA replication an phospholipid synthesis in Caulobacter crescentus.

Authors: L Shapiro; J Mansour; P Shaw; S Henry
Journal: J Mol Biol Date: 1982-08-05 Impact factor: 5.469

2. Localization of the Escherichia coli RNA polymerase beta' subunit residue phosphorylated by bacteriophage T7 kinase Gp0.7.

Authors: Elena Severinova; Konstantin Severinov
Journal: J Bacteriol Date: 2006-05 Impact factor: 3.490

2 in total

Phosphorylation of the beta' Subunit of RNA Polymerase and Other Host Proteins upon phiCd1 Infection of Caulobacter crescentus.

1. BIOLOGICAL PROPERTIES AND CLASSIFICATION OF THE CAULOBACTER GROUP.

2. Caulobacter crescentus RNA polymerase. Purification and characterization of holoenzyme and core polymerase.

3. Control of gene expression in bacteriophage T7: transcriptional controls.

4. Characterization of a protein acyl kinase from Caulobacter crescentus.

5. RNase III is positively regulated by T7 protein kinase.

6. Physical map of Caulobacter crescentus bacteriophage phi Cd1 DNA.

7. Synthesis of specific membrane proteins is a function of DNA replication an phospholipid synthesis in Caulobacter crescentus.

8. Isolation and characterization of Caulobacter crecentus bacteriophage phi Cd1.

9. T7 early RNAs and Escherichia coli ribosomal RNAs are cut from large precursor RNAs in vivo by ribonuclease 3.

10. Heterogeneity of RNA polymerase in Bacillus subtilis: evidence for an additional sigma factor in vegetative cells.

1. Effect of protein phosphorylation on the activity of RNA polymerase in streptomycetes.

2. Localization of the Escherichia coli RNA polymerase beta' subunit residue phosphorylated by bacteriophage T7 kinase Gp0.7.