Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach. (Articolo in rivista)

Type
Label
  • Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach. (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Alternative label
  • Facchiano A, Marabotti A. (2010)
    Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach.
    in Protein engineering, design & selection (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Facchiano A, Marabotti A. (literal)
Pagina inizio
  • 103 (literal)
Pagina fine
  • 113 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • PMID: 20008339 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 23 (literal)
Rivista
Note
  • PubMe (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Scienze dell'Alimentazione, CNR, Avellino (literal)
Titolo
  • Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach. (literal)
Abstract
  • We describe the prediction of the structural and functional effects of mutations on the enzyme galactose-1-phosphate uridyltransferase related to the genetic disease galactosemia, using a fully computational approach. One hundred and seven single-point mutants were simulated starting from the structural model of the enzyme obtained by homology modeling methods. Several bioinformatics programs were then applied to each resulting mutant protein to analyze the effect of the mutations. The mutations have a direct effect on the active site, or on the dimer assembly and stability, or on the monomer stability. We describe how mutations may exert their effect at a molecular level by altering H-bonds, salt bridges, secondary structure or surface features. The alteration of protein stability, at level of monomer and/or dimer, is the main effect observed. We found an agreement between our results and the functional experimental data available in literature for some mutants. The data and analyses for all the mutants are fully available in the web-accessible database hosted at http://bioinformatica.isa.cnr.it/GALT (literal)
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