Difference between revisions of "GapA"
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=== Database entries === | === Database entries === | ||
+ | * '''BsubCyc:''' [http://bsubcyc.org/BSUB/NEW-IMAGE?type=NIL&object=BSU33940&redirect=T BSU33940] | ||
* '''DBTBS entry:''' [http://dbtbs.hgc.jp/COG/prom/cggR-gapA-pgk-tpiA-pgm-eno.html] | * '''DBTBS entry:''' [http://dbtbs.hgc.jp/COG/prom/cggR-gapA-pgk-tpiA-pgm-eno.html] | ||
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=== Database entries === | === Database entries === | ||
+ | * '''BsubCyc:''' [http://bsubcyc.org/BSUB/NEW-IMAGE?type=NIL&object=BSU33940&redirect=T BSU33940] | ||
* '''Structure:''' | * '''Structure:''' |
Revision as of 14:47, 2 April 2014
- Description: Glyceraldehyde 3-phosphate dehydrogenase, NAD-dependent, glycolytic enzyme, forms a transhydrogenation cycle with GapB for balancing of NADPH
Gene name | gapA |
Synonyms | |
Essential | Yes (PubMed) |
Product | glyceraldehyde 3-phosphate dehydrogenase |
Function | catabolic enzyme in glycolysis |
Gene expression levels in SubtiExpress: gapA | |
Interactions involving this protein in SubtInteract: GapA | |
Metabolic function and regulation of this protein in SubtiPathways: gapA | |
MW, pI | 35.7 kDa, 5.03 |
Gene length, protein length | 1005 bp, 335 amino acids |
Immediate neighbours | pgk, cggR |
Sequences | Protein DNA DNA_with_flanks |
Genetic context This image was kindly provided by SubtiList
| |
Expression at a glance PubMed |
Contents
Categories containing this gene/protein
carbon core metabolism, essential genes, membrane proteins, phosphoproteins, most abundant proteins
This gene is a member of the following regulons
The gene
Basic information
- Locus tag: BSU33940
Phenotypes of a mutant
- Essential PubMed
Database entries
- BsubCyc: BSU33940
- DBTBS entry: [1]
- SubtiList entry:[2]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: D-glyceraldehyde 3-phosphate + phosphate + NAD+ = 3-phospho-D-glyceroyl phosphate + NADH (according to Swiss-Prot)
- 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: Michaelis-Menten PubMed
- Modification:
- Effectors of protein activity:
Database entries
- BsubCyc: BSU33940
- Structure:
- UniProt: P09124
- KEGG entry: [3]
- 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).
- extensive information on the structure and enzymatic properties of GapA can be found at Proteopedia
Expression and regulation
- 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)
- belongs to the 100 most abundant proteins PubMed
- 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. PubMed The processing event requires the RNase Y PubMed.
- The accumulation of the cggR-gapA mRNA is strongly dependent on the presence of the YkzW peptide, due to stabilization of the mRNA PubMed.
- the mRNA is substantially stabilized upon depletion of RNase Y PubMed
Biological materials
- Mutant:
- GP592 (gapA::cat), available in Jörg Stülke's lab, PubMed
- GP597 (gapA::erm), available in Jörg Stülke's lab, PubMed
- GP703 (gapA::cat gapB::spec), available in Jörg Stülke's lab, PubMed
- GM1501 (under p(spac) control), available in Stephane Aymerich's lab
- 1A1003 ( gapA::erm), available at BGSC
- Expression vector:
- pGP1424 (expression in B. subtilis, in pBQ200) (available in Jörg Stülke's lab)
- pGP90 (N-terminal Strep-tag, for SPINE, purification from B. subtilis, in pGP380) (available in Jörg Stülke's lab)
- pGP704 (N-terminal His-tag, in pWH844) (available in Jörg Stülke's lab)
- lacZ fusion: pGP506 (in pAC7), pGP512 (in pAC6) (available in Jörg Stülke's lab)
- GFP fusion:
- two-hybrid system: B. pertussis adenylate cyclase-based bacterial two hybrid system (BACTH), available in Jörg Stülke's lab
- Antibody: available in Jörg Stülke's 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