Difference between revisions of "HypO"
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* '''Operon:''' ''hypO'' {{PubMed|22238377}} | * '''Operon:''' ''hypO'' {{PubMed|22238377}} | ||
− | * '''[ | + | * '''Expression browser:''' [http://genome.jouy.inra.fr/cgi-bin/seb/viewdetail.py?id=yfkO_854412_855077_1 hypO] {{PubMed|22383849}} |
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+ | * '''Sigma factor:''' [[SigA]] {{PubMed|22238377}} | ||
* '''Regulation:''' | * '''Regulation:''' |
Revision as of 16:09, 12 April 2012
- Description: NAD(P)H-flavin nitroreductase
Gene name | hypO |
Synonyms | yfkO |
Essential | no |
Product | NAD(P)H-flavin nitroreductase |
Function | protection against NaOCl stress |
MW, pI | 25 kDa, 5.667 |
Gene length, protein length | 663 bp, 221 aa |
Immediate neighbours | treR, yfkN |
Get the DNA and protein sequences (Barbe et al., 2009) | |
Genetic context This image was kindly provided by SubtiList
|
Contents
Categories containing this gene/protein
electron transport/ other, resistance against oxidative and electrophile stress
This gene is a member of the following regulons
The gene
Basic information
- Locus tag: BSU07830
Phenotypes of a mutant
Database entries
- DBTBS entry: [1]
- SubtiList entry: [2]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity:
- Protein family: nitroreductase family (according to Swiss-Prot)
- Paralogous protein(s):
Extended information on the protein
- Kinetic information:
- Domains:
- Modification:
- Cofactor(s):
- Effectors of protein activity:
Database entries
- Structure:
- UniProt: O34475
- KEGG entry: [3]
- E.C. number:
Additional information
Expression and regulation
- Operon: hypO PubMed
- Additional information:
Biological materials
- Mutant:
- Expression vector:
- lacZ fusion:
- GFP fusion:
- two-hybrid system:
- Antibody:
Labs working on this gene/protein
- Haike Antelmann, University of Greifswald, Germany
Your additional remarks
References
Original articles
G A Prosser, A V Patterson, D F Ackerley
uvrB gene deletion enhances SOS chromotest sensitivity for nitroreductases that preferentially generate the 4-hydroxylamine metabolite of the anti-cancer prodrug CB1954.
J Biotechnol: 2010, 150(1);190-4
[PubMed:20727918]
[WorldCat.org]
[DOI]
(I p)
Palm GJ, Khanh Chi B, Waack P, Gronau K, Becher D, Albrecht D, Hinrichs W, Read RJ, Antelmann H. Structural insights into the redox-switch mechanism of the MarR/DUF24-type regulator HypR. Nucleic Acids Res. 2012, Jan 11. [Epub ahead of print] PubMed