Literature DB >> 6554278

P22 c2 repressor. Domain structure and function.

J De Anda, A R Poteete, R T Sauer.   

Abstract

The c2 repressor of bacteriophage P22 can be digested with trypsin, chymotrypsin, or elastase to yield stable fragments. Purified NH2-terminal fragments, like intact repressor, bind specifically to P22 operator DNA and also mediate positive and negative control of transcription. COOH-terminal fragments of repressor do not bind operator DNA but do undergo a concentration-dependent oligomerization similar to that observed with intact repressor. These results suggest that P22 repressor, like the related cI repressor of phage lambda, contains two structural domains which mediate different functions of the intact molecule.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6554278

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  22 in total

1.  The preferred substrate for RecA-mediated cleavage of bacteriophage 434 repressor is the DNA-bound dimer.

Authors:  David R Pawlowski; Gerald B Koudelka
Journal:  J Bacteriol       Date:  2004-01       Impact factor: 3.490

2.  pH-dependent autocleavage of lambda repressor occurs in the operator-bound form: characterization of lambda repressor autocleavage.

Authors:  Kaushik Ghosh; Atasi Pal; Rajagopal Chattopadhyaya
Journal:  Biochem J       Date:  2004-04-15       Impact factor: 3.857

3.  Structural analysis of the carboxy terminus of bacteriophage lambda repressor determined by antipeptide antibodies.

Authors:  R Sussman; H B Alexander
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

4.  The bacteriophage 434 repressor dimer preferentially undergoes autoproteolysis by an intramolecular mechanism.

Authors:  Barbara C McCabe; David R Pawlowski; Gerald B Koudelka
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

5.  Effect of salt shock on stability of lambdaimm434 lysogens.

Authors:  Paul Shkilnyj; Gerald B Koudelka
Journal:  J Bacteriol       Date:  2007-02-16       Impact factor: 3.490

6.  Dimerization specificity of P22 and 434 repressors is determined by multiple polypeptide segments.

Authors:  A L Donner; P A Carlson; G B Koudelka
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

7.  Structure of a hyper-cleavable monomeric fragment of phage lambda repressor containing the cleavage site region.

Authors:  Dieudonné Ndjonka; Charles E Bell
Journal:  J Mol Biol       Date:  2006-07-15       Impact factor: 5.469

8.  Mutant LexA proteins with specific defects in autodigestion.

Authors:  D P Shepley; J W Little
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

Review 9.  Bacteriophage protein-protein interactions.

Authors:  Roman Häuser; Sonja Blasche; Terje Dokland; Elisabeth Haggård-Ljungquist; Albrecht von Brunn; Margarita Salas; Sherwood Casjens; Ian Molineux; Peter Uetz
Journal:  Adv Virus Res       Date:  2012       Impact factor: 9.937

10.  Specificity of a retinoic acid response element in the phosphoenolpyruvate carboxykinase gene promoter: consequences of both retinoic acid and thyroid hormone receptor binding.

Authors:  P C Lucas; B M Forman; H H Samuels; D K Granner
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.