Difference between revisions of "LicR"
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=== Basic information/ Evolution === | === Basic information/ Evolution === | ||
− | * '''Catalyzed reaction/ biological activity:''' | + | * '''Catalyzed reaction/ biological activity:''' Protein EIIA N(pi)-phospho-L-histidine + protein EIIB = protein EIIA + protein EIIB N(pi)-phospho-L-histidine/cysteine (according to Swiss-Prot) |
* '''Protein family:''' transcriptional antiterminator bglG family (according to Swiss-Prot) | * '''Protein family:''' transcriptional antiterminator bglG family (according to Swiss-Prot) |
Revision as of 16:49, 24 May 2009
- Description: transcriptional activator of the licB-licC-licA-licH operon
Gene name | licR |
Synonyms | celR |
Essential | no |
Product | transcriptional activator (PRD type) |
Function | regulation of lichenan utilization |
MW, pI | 73 kDa, 6.115 |
Gene length, protein length | 1923 bp, 641 aa |
Immediate neighbours | licB, yxzF |
Get the DNA and protein sequences (Barbe et al., 2009) | |
Genetic context This image was kindly provided by SubtiList
|
Contents
The gene
Basic information
- Coordinates:
Phenotypes of a mutant
Database entries
- DBTBS entry: [1]
- SubtiList entry: [2]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: Protein EIIA N(pi)-phospho-L-histidine + protein EIIB = protein EIIA + protein EIIB N(pi)-phospho-L-histidine/cysteine (according to Swiss-Prot)
- Protein family: transcriptional antiterminator bglG family (according to Swiss-Prot)
- Paralogous protein(s):
Extended information on the protein
- Kinetic information:
- Domains:
- Modification:
- Cofactor(s):
- Effectors of protein activity:
- Localization:
Database entries
- Structure:
- Swiss prot entry: P46321
- KEGG entry: BSU38600
- E.C. number: 2.7.1.69
Additional information
Expression and regulation
- Operon:
- Regulation:
- Regulatory mechanism:
- Additional information:
Biological materials
- Mutant:
- Expression vector:
- lacZ fusion:
- GFP fusion:
- two-hybrid system:
- Antibody:
Labs working on this gene/protein
Your additional remarks
References
- Tobisch, S., P. Glaser, S. Krüger, and M. Hecker. 1997. Identification and characterization of a new ß-glucoside utilization system in Bacillus subtilis. J. Bacteriol. 179:496-506. PubMed
- Tobisch, S., Stülke, J., & Hecker, M. (1999) Regulation of the lic operon of Bacillus subtilis and characterization of potential phosphorylation sites of the LicR regulator protein by site-directed mutagenesis. J. Bacteriol. 181: 4995-5003. PubMed
- Author1, Author2 & Author3 (year) Title Journal volume: page-page. PubMed