Literature DB >> 3625774

Systematic method for the detection of potential lambda Cro-like DNA-binding regions in proteins.

I B Dodd, J B Egan.   

Abstract

We have developed and tested a systematic method for the location and statistical evaluation of potential DNA-binding regions of the lambda Cro type in protein sequences. Using this approach to examine proteins expected to contain such regions, we have been able to compile a statistically homogeneous master set of 37 lambda Cro-like DNA-binding domains. Examination of a protein database revealed other prokaryotic proteins that are similar to this lambda Cro-like group. There are also many DNA-binding proteins that are not found to be significantly similar to the lambda Cro group, consistent with previous suggestions that different types of protein sequence may be able to achieve a similar mode of binding and that there exist other modes of sequence-specific DNA-binding. A useful feature of the method is that it can be applied without a computer.

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Year:  1987        PMID: 3625774     DOI: 10.1016/0022-2836(87)90681-4

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  82 in total

1.  Genetic organization of the citCDEF locus and identification of mae and clyR genes from Leuconostoc mesenteroides.

Authors:  S Bekal-Si Ali; C Diviès; H Prévost
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Genetic analysis of the LexA repressor: isolation and characterization of LexA(Def) mutant proteins.

Authors:  P Oertel-Buchheit; R M Lamerichs; M Schnarr; M Granger-Schnarr
Journal:  Mol Gen Genet       Date:  1990-08

3.  Gene F of plasmid RSF1010 codes for a low-molecular-weight repressor protein that autoregulates expression of the repAC operon.

Authors:  S Maeser; P Scholz; S Otto; E Scherzinger
Journal:  Nucleic Acids Res       Date:  1990-11-11       Impact factor: 16.971

4.  Cloning, sequencing and analysis of the structural gene and regulatory region of the Pseudomonas aeruginosa chromosomal ampC beta-lactamase.

Authors:  J M Lodge; S D Minchin; L J Piddock; S J Busby
Journal:  Biochem J       Date:  1990-12-15       Impact factor: 3.857

5.  Nucleotide sequence and transcriptional analysis of activator-regulator proteins for beta-lactamase in Streptomyces cacaoi.

Authors:  H Urabe; H Ogawara
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

6.  Nucleotide sequencing and characterization of Pseudomonas putida catR: a positive regulator of the catBC operon is a member of the LysR family.

Authors:  R K Rothmel; T L Aldrich; J E Houghton; W M Coco; L N Ornston; A M Chakrabarty
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

7.  Evidence that the transcription activator encoded by the Pseudomonas putida nahR gene is evolutionarily related to the transcription activators encoded by the Rhizobium nodD genes.

Authors:  M A Schell; M Sukordhaman
Journal:  J Bacteriol       Date:  1989-04       Impact factor: 3.490

Review 8.  The leucine-responsive regulatory protein, a global regulator of metabolism in Escherichia coli.

Authors:  J M Calvo; R G Matthews
Journal:  Microbiol Rev       Date:  1994-09

9.  Molecular cloning and nucleotide sequencing of oxyR, the positive regulatory gene of a regulon for an adaptive response to oxidative stress in Escherichia coli: homologies between OxyR protein and a family of bacterial activator proteins.

Authors:  K Tao; K Makino; S Yonei; A Nakata; H Shinagawa
Journal:  Mol Gen Genet       Date:  1989-09

10.  Cloning and characterization of the A-factor receptor gene from Streptomyces griseus.

Authors:  H Onaka; N Ando; T Nihira; Y Yamada; T Beppu; S Horinouchi
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

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