Difference between revisions of "GlnA"

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** GP247 (''glnA::cat''), available in [[Jörg Stülke]]'s lab  
 
** GP247 (''glnA::cat''), available in [[Jörg Stülke]]'s lab  
 
** BP148 (del(''[[glnR]]-[[glnA]]'')::''cat''), available in [[Fabian Commichau]]'s lab
 
** BP148 (del(''[[glnR]]-[[glnA]]'')::''cat''), available in [[Fabian Commichau]]'s lab
 +
** GP1883 (del(''[[glnR]]-[[glnA]]'')::''ermC''), available in [[Fabian Commichau]]'s and [[Jörg Stülke]]'s labs
  
 
* '''Expression vector:'''
 
* '''Expression vector:'''

Revision as of 08:18, 24 September 2014

Gene name glnA
Synonyms
Essential no
Product trigger enzyme: glutamine synthetase
Function glutamine biosynthesis, control of TnrA and GlnR activity
Gene expression levels in SubtiExpress: glnA
Interactions involving this protein in SubtInteract: GlnA
Metabolic function and regulation of this protein in SubtiPathways:
glnA
MW, pI 50 kDa, 4.874
Gene length, protein length 1332 bp, 444 aa
Immediate neighbours glnR, ynxB
Sequences Protein DNA DNA_with_flanks
Genetic context
GlnA context.gif
This image was kindly provided by SubtiList
Expression at a glance   PubMed
GlnA expression.png















Categories containing this gene/protein

biosynthesis/ acquisition of amino acids, glutamate metabolism, transcription factors and their control, trigger enzyme, phosphoproteins, most abundant proteins

This gene is a member of the following regulons

GlnR regulon, TnrA regulon

The gene

Basic information

  • Locus tag: BSU17460

Phenotypes of a mutant

auxotrophic for glutamine

Database entries

  • DBTBS entry: [1]
  • SubtiList entry: [2]

Additional information

The protein

Basic information/ Evolution

  • Catalyzed reaction/ biological activity: ATP + L-glutamate + NH3 = ADP + phosphate + L-glutamine (according to Swiss-Prot)
  • Protein family: glutamine synthetase family (according to Swiss-Prot)
  • Paralogous protein(s):

Extended information on the protein

  • Kinetic information: K(M) for: Glu: 27 mM, ATP: 2.4 mM, ammonium: 0.18 mM; v(max): 3.7 µmol/min/mg
  • Domains: glutamate binding flap (aa 300 ... 306: protects unstable intermediates from abberant hydrolysis)
  • Modification:
    • phosphorylated on ser/ thr/ tyr PubMed
    • in vitro phosphorylated by PrkC on Thr-26, Thr-147, Ser-207, and Thr-286 PubMed
  • Effectors of protein activity:
    • feedback inhibition by glutamine, glutamine binds the entrance site for glutamate
    • activity is inhibited upon interaction with TnrA PubMed

Database entries

  • KEGG entry: [3]

Additional information

GlnA is a homooligomer of 12 subunits

Expression and regulation

  • Regulation:
    • expressed in the absence of glutamine (GlnR) PubMed
    • repressed in the absence of good nitrogen sources (glutamine or ammonium) (TnrA) PubMed
  • Additional information:
    • belongs to the 100 most abundant proteins PubMed
    • number of protein molecules per cell (minimal medium with glucose and ammonium): 8140 PubMed
    • number of protein molecules per cell (complex medium with amino acids, without glucose): 11334 PubMed
    • number of protein molecules per cell (minimal medium with glucose and ammonium, exponential phase): 16645 PubMed
    • number of protein molecules per cell (minimal medium with glucose and ammonium, early stationary phase after glucose exhaustion): 11115 PubMed
    • number of protein molecules per cell (minimal medium with glucose and ammonium, late stationary phase after glucose exhaustion): 11598 PubMed

Biological materials

  • Expression vector:
    • expression/ purification from E. coli, with N-terminal Strep-tag (in pGP172): pGP174, available in Jörg Stülke's lab
    • pGP177 (N-terminal Strep-tag, purification from B. subtilis, for SPINE, in pBQ200), available in Jörg Stülke's lab
  • GFP fusion:
  • two-hybrid system:

Labs working on this gene/protein

Susan Fisher, Boston, USA homepage

Your additional remarks

References

Reviews


Original publications