Difference between revisions of "GapA"
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Revision as of 08:00, 23 May 2009
- Description: Glyceraldehyde 3-phosphate dehydrogenase, NAD-dependent, glycolytic enzyme
Gene name | gapA |
Synonyms | |
Essential | Yes (PubMed) |
Product | glyceraldehyde 3-phosphate dehydrogenase |
Function | catabolic enzyme in glycolysis |
MW, pI | 35.7 kDa, 5.03 |
Gene length, protein length | 1005 bp, 335 amino acids |
Immediate neighbours | cggR, pgk |
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: 3480732 - 3481736
Phenotypes of a mutant
essential PubMed
Database entries
- DBTBS entry: [1]
- SubtiList entry:[2]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: glyceraldehyde-3-phosphate dehydrogenase, (NADH-dependent). Catalyzes the reaction from glyceraldehyde-3-phosphate to 1.3-bi-phosphoglycerate. This reaction is part of the glycolysis.
- Protein family: glyceraldehyde-3-phosphate dehydrogenase family (according to Swiss-Prot)
- Paralogous protein(s): GapB
Extended information on the protein
- Kinetic information: K(M) for NAD: 5.7 mM, K(cat) for NAD: 70/sec (determined for GapA from Geobacillus stearothermophilus) PubMed
- Domains:
- Cofactor(s):
- Effectors of protein activity:
- Interactions:
- GapA-PtsH: HPr(Ser-46-P) binds GapA resulting in a slight inhibition of enzymatic activity.PubMed
- GapA-Crh: Crh(Ser-46-P) binds GapA resulting in a slight inhibition of enzymatic activity.PubMed
- Localization: cytoplasm (according to Swiss-Prot), Cytoplasm (Homogeneous) PubMed PubMed, loosely membrane associated PubMed
Database entries
- Structure:
- Swiss prot entry: P09124
- KEGG entry: BSU33940
- E.C. number: 1.2.1.12
Additional information
GAP dehydrogenases from different sources (incl. Geobacillus stearothermophilus) were shown to cleave RNA (PubMed). Moreover, mutations in gapA from B. subtilis can suppress mutations in genes involved in DNA replication (PubMed).
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. The processing event requires the Rny protein.
- Sigma factor: SigA
- Regulation: expression activated by glucose (10 fold) PubMed, CggR represses the operon in the absence of glycolytic sugars PubMed
- Regulatory mechanism: repression
- Database entries: DBTBS
- Additional information: GapA is one of the most abundant proteins in the cell. In the presence of glucose, there are about 25,000 GapA molecules per cell (PubMed).
Biological materials
- Mutant: essential
- Expression vector: pGP90 (N-terminal Strep-tag, for SPINE, purification from B. subtilis, in pGP380), pGP704 (N-terminal His-tag, in pWH844) (available in Stülke lab)
- GFP fusion:
- two-hybrid system: B. pertussis adenylate cyclase-based bacterial two hybrid system (BACTH), available in Stülke lab
- Antibody: available in Stülke lab
Labs working on this gene/protein
Stephane Aymerich, Microbiology and Molecular Genetics, INRA Paris-Grignon, France
Jörg Stülke, University of Göttingen, Germany homepage
Your additional remarks
References