Molecular cloning of cDNA and analysis of protein secondary structure of Candida albicans enolase, an abundant, immunodominant glycolytic enzyme.

We isolated and sequenced a clone for Candida albicans enolase from a C. albicans cDNA library by using molecular genetic techniques. The 1.4-kbp cDNA encoded one long open reading frame of 440 amino acids which was 87 and 75% similar to predicted enolases of Saccharomyces cerevisiae and enolases fr...

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Veröffentlicht in:	J Bacteriol
Hauptverfasser:	Sundstrom, P, Aliaga, G R
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Microbiology (ASM) 1992
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC207354/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1400228/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.174.21.6789-6799.1992
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