Difference between revisions of "GapA"
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(→Expression and regulation) |
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** ''[[cggR]]-[[gapA]]'' | ** ''[[cggR]]-[[gapA]]'' | ||
− | The primary mRNAs of the operon are highly unstable. The primary mRNA is subject to processing at the very end of the [[''cggR'']] open reading frame. This results in stable mature ''gapA'' and ''gapA-[[pgk]]-[[tpiA]]-[[pgm]]-[[eno]]'' mRNAs. | + | The primary mRNAs of the operon are highly unstable. The primary mRNA is subject to processing at the very end of the [[''cggR'']] open reading frame. This results in stable mature ''[[gapA]]'' and ''[[gapA]]-[[pgk]]-[[tpiA]]-[[pgm]]-[[eno]]'' mRNAs. |
* '''Sigma factor:''' SigA | * '''Sigma factor:''' SigA |
Revision as of 17:09, 12 December 2008
- Synonyms:
- Description: glyceraldehyde-3-phosphate dehydrogenase, (NADH-dependent), glycolytic enzyme
Contents
The gene
Basic information
- Coordinates:
- Gene length:
Phenotypes of a mutant
essential
Database entries
- DBTBS entry: [1]
- SubtiList entry:[2]
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: glyceraldehyde-3-phosphate dehydrogenase, (NADH-dependent)
- Protein family:
- Paralogous protein(s): GapB
Extended information on the protein
- Kinetic information:
- Domains:
- Modification: Phosphorylation (STY)
- Effectors of protein activity:
- Interactions:
- GapA-PtsH: HPr(Ser-46-P) binds GapA resulting in a slight inhibition of enzymatic activity.
- GapA-Crh: Crh(Ser-46-P) binds GapA resulting in a slight inhibition of enzymatic activity.
- Localization: membrane and cytoplasm
Database entries
- Structure:
- Swiss prot entry: P09124
- KEGG entry: KEGG
Expression and regulation
The primary mRNAs of the operon are highly unstable. The primary mRNA is subject to processing at the very end of the ''cggR'' open reading frame. This results in stable mature gapA and gapA-pgk-tpiA-pgm-eno mRNAs.
- Sigma factor: SigA
- Regulation: CggR represses the operon in the absence of glycolytic sugars
- Regulatory mechanism: repression
- Database entries: DBTBS
Biological materials
- Mutant:
- Expression vector:
- lacZ fusion:
- GFP fusion:
- Antibody:
Labs working on this gene/protein
Your additional remarks
References
- Author1, Author2 & Author3 (year) Title Journal volume: page-page. [3]