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FBA1  -  fructose-bisphosphate aldolase FBA1

Saccharomyces cerevisiae S288c

Synonyms: FBP aldolase, FBPA, Fructose-1,6-bisphosphate aldolase, Fructose-bisphosphate aldolase, YKL060C, ...
 
 
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Disease relevance of FBA1

  • From the genomic clones a yeast/Escherichia coli shuttle plasmid was constructed containing on a 1990-base-pair fragment the entire structural gene FBA1 coding for yeast aldolase [1].
  • Taken together, our observations can account for our observation that the virulence of MET3-FBA1/fba1 cells is only partially attenuated in the mouse model of systemic candidiasis [2].
 

High impact information on FBA1

  • Yeast D-fructose bisphosphate aldolase appears to utilize both alpha and beta anomers of the substrate, with yeast apoaldolase catalyzing the interconversion of the alpha and beta forms [3].
  • From a series of rapid quench kinetic experiments, it has been demonstrated that muscle D-fructose bisphosphate aldolase catalyzes the cleavage of beta-D-fructose 1,6-bisphosphate but not that of the alpha anomer, although the alpha anomer may be tightly bound [3].
  • A FBA1::lacZ gene fusion was constructed and a deletion analysis demonstrated the presence of a unique cis-acting positive upstream element (UAS) required for high levels of FBA1 expression [4].
  • In addition, all the LOT genes, except for LOT1/FBA1, were induced by a low concentration of cycloheximide [5].
  • Sequence of a 28.6 kb region of yeast chromosome XI includes the FBA1 and TOA2 genes, an open reading frame (ORF) similar to a translationally controlled tumour protein, one ORF containing motifs also found in plant storage proteins and 13 ORFs with weak or no homology to known proteins [6].
 

Biological context of FBA1

  • Aldolase is the major protein in yeast cells transformed with a high-copy-number plasmid containing the FBA1 gene [1].
  • The 810 base pairs at the 5' end and the 90 base pairs at the 3' end of the coding region of the cloned FBA1 gene are sufficient for normal expression and show characteristic elements present in the noncoding sequences of other yeast genes [1].
  • The aldolase gene was disrupted by insertion of the yeast URA3 gene into the coding region of one FBA1 allele in a homozygous diploid ura3 strain [1].
  • The central metabolic enzyme fructose-1,6-bisphosphate aldolase (Fba1p) catalyzes a reversible reaction required for both glycolysis and gluconeogenesis [2].
 

Associations of FBA1 with chemical compounds

References

  1. Molecular cloning, primary structure and disruption of the structural gene of aldolase from Saccharomyces cerevisiae. Schwelberger, H.G., Kohlwein, S.D., Paltauf, F. Eur. J. Biochem. (1989) [Pubmed]
  2. Effects of depleting the essential central metabolic enzyme fructose-1,6-bisphosphate aldolase on the growth and viability of Candida albicans: implications for antifungal drug target discovery. Rodaki, A., Young, T., Brown, A.J. Eukaryotic Cell (2006) [Pubmed]
  3. The anomeric form of D-fructose 1,6-bisphosphate used as substrate in the muscle and yeast aldolase reactions. Schray, K.J., Fishbein, R., Bullard, W.P., Benkovic, S.J. J. Biol. Chem. (1975) [Pubmed]
  4. The promoter of Saccharomyces cerevisiae FBA1 gene contains a single positive upstream regulatory element. Compagno, C., Ranzi, B.M., Martegani, E. FEBS Lett. (1991) [Pubmed]
  5. Multiple mechanisms regulate expression of low temperature responsive (LOT) genes in Saccharomyces cerevisiae. Zhang, L., Ohta, A., Horiuchi, H., Takagi, M., Imai, R. Biochem. Biophys. Res. Commun. (2001) [Pubmed]
  6. Sequence of a 28.6 kb region of yeast chromosome XI includes the FBA1 and TOA2 genes, an open reading frame (ORF) similar to a translationally controlled tumour protein, one ORF containing motifs also found in plant storage proteins and 13 ORFs with weak or no homology to known proteins. Rasmussen, S.W. Yeast (1994) [Pubmed]
  7. Isolation and transcriptional regulation of the Kluyveromyces lactis FBA1 (fructose-1,6-bisphosphate aldolase) gene. Prado, S.M., Cerdán, M.E., González Siso, M.I. Can. J. Microbiol. (2004) [Pubmed]
 
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