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1.
Nucleic Acids Res ; 32(18): 5539-45, 2004.
Article in English | MEDLINE | ID: mdl-15486203

ABSTRACT

In this paper, we present the Functional Catalogue (FunCat), a hierarchically structured, organism-independent, flexible and scalable controlled classification system enabling the functional description of proteins from any organism. FunCat has been applied for the manual annotation of prokaryotes, fungi, plants and animals. We describe how FunCat is implemented as a highly efficient and robust tool for the manual and automatic annotation of genomic sequences. Owing to its hierarchical architecture, FunCat has also proved to be useful for many subsequent downstream bioinformatic applications. This is illustrated by the analysis of large-scale experiments from various investigations in transcriptomics and proteomics, where FunCat was used to project experimental data into functional units, as 'gold standard' for functional classification methods, and also served to compare the significance of different experimental methods. Over the last decade, the FunCat has been established as a robust and stable annotation scheme that offers both, meaningful and manageable functional classification as well as ease of perception.


Subject(s)
Computational Biology/methods , Genome , Proteins/classification , Proteins/metabolism , Proteomics/methods , Software , Abstracting and Indexing , Animals , Automation/instrumentation , Automation/methods , Computational Biology/instrumentation , Genomics/instrumentation , Genomics/methods , Internet , Protein Binding , Proteins/genetics , Proteome/classification , Proteome/genetics , Proteome/metabolism , Proteomics/instrumentation , Reproducibility of Results , Saccharomyces cerevisiae/chemistry , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/classification , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism , Terminology as Topic , Transcription, Genetic/genetics
2.
FEMS Yeast Res ; 4(2): 207-15, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14613885

ABSTRACT

The methylotrophic yeast Hansenula polymorpha is a recognised model system for investigation of peroxisomal function, special metabolic pathways like methanol metabolism, of nitrate assimilation or thermostability. Strain RB11, an odc1 derivative of the particular H. polymorpha isolate CBS4732 (synonymous to ATCC34438, NRRL-Y-5445, CCY38-22-2) has been developed as a platform for heterologous gene expression. The scientific and industrial significance of this organism is now being met by the characterisation of its entire genome. The H. polymorpha RB11 genome consists of approximately 9.5 Mb and is organised as six chromosomes ranging in size from 0.9 to 2.2 Mb. Over 90% of the genome was sequenced with concomitant high accuracy and assembled into 48 contigs organised on eight scaffolds (supercontigs). After manual annotation 4767 out of 5933 open reading frames (ORFs) with significant homologies to a non-redundant protein database were predicted. The remaining 1166 ORFs showed no significant similarity to known proteins. The number of ORFs is comparable to that of other sequenced budding yeasts of similar genome size.


Subject(s)
Genome, Fungal , Pichia/genetics , Sequence Analysis, DNA , Base Sequence , DNA, Fungal/genetics , Databases, Protein , Gene Library , Genes, Fungal , Molecular Sequence Data , Open Reading Frames/genetics , Saccharomyces cerevisiae/genetics
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