Difference between revisions of "EpsL"

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* '''Regulation:'''  
 
* '''Regulation:'''  
 +
** repressed by [[SinR]] [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]
  
 
* '''Regulatory mechanism:''' [[SinR]]: transcription repression [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]
 
* '''Regulatory mechanism:''' [[SinR]]: transcription repression [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]
 +
** [[SinR]]: transcription repression [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]
  
 
* '''Additional information:''' induction by sequestration of [[SinR]] by [[SinI]] [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]
 
* '''Additional information:''' induction by sequestration of [[SinR]] by [[SinI]] [http://www.ncbi.nlm.nih.gov/sites/entrez/15661000 PubMed]

Revision as of 17:22, 11 June 2009

  • Description: similar to UDP-galactose phosphate transferase, extracellular polysaccharide synthesis

Gene name epsL
Synonyms yvfC
Essential no
Product unknown
Function extracellular polysaccharide synthesis
MW, pI 22 kDa, 9.973
Gene length, protein length 606 bp, 202 aa
Immediate neighbours epsM, epsK
Get the DNA and protein sequences
(Barbe et al., 2009)
Genetic context
YvfC context.gif
This image was kindly provided by SubtiList



The gene

Basic information

  • Locus tag: BSU34250

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: bacterial sugar transferase family (according to Swiss-Prot)
  • Paralogous protein(s): TuaA

Extended information on the protein

  • Kinetic information:
  • Domains:
  • Modification:
  • Cofactor(s):
  • Effectors of protein activity:
  • Interactions:
  • Localization: cell membrane (according to Swiss-Prot)

Database entries

  • Structure:
  • KEGG entry: [3]
  • E.C. number:

Additional information

Expression and regulation

  • Additional information: induction by sequestration of SinR by SinI PubMed

Biological materials

  • Mutant:
  • Expression vector:
  • lacZ fusion:
  • GFP fusion:
  • two-hybrid system:
  • Antibody:

Labs working on this gene/protein

Richard Losick, Harvard Univ., Cambridge, USA homepage

Your additional remarks

References


  1. Author1, Author2 & Author3 (year) Title Journal volume: page-page. PubMed