Literature DB >> 24990533

GALT protein database: querying structural and functional features of GALT enzyme.

Antonio d'Acierno1, Angelo Facchiano, Anna Marabotti.   

Abstract

Knowledge of the impact of variations on protein structure can enhance the comprehension of the mechanisms of genetic diseases related to that protein. Here, we present a new version of GALT Protein Database, a Web-accessible data repository for the storage and interrogation of structural effects of variations of the enzyme galactose-1-phosphate uridylyltransferase (GALT), the impairment of which leads to classic Galactosemia, a rare genetic disease. This new version of this database now contains the models of 201 missense variants of GALT enzyme, including heterozygous variants, and it allows users not only to retrieve information about the missense variations affecting this protein, but also to investigate their impact on substrate binding, intersubunit interactions, stability, and other structural features. In addition, it allows the interactive visualization of the models of variants collected into the database. We have developed additional tools to improve the use of the database by nonspecialized users. This Web-accessible database (http://bioinformatica.isa.cnr.it/GALT/GALT2.0) represents a model of tools potentially suitable for application to other proteins that are involved in human pathologies and that are subjected to genetic variations.
© 2014 WILEY PERIODICALS, INC.

Entities:  

Keywords:  Classic Galactosemia; GALT; database; galactose-1-phosphate uridylyltransferase; molecular modelling; structural analysis

Mesh:

Substances:

Year:  2014        PMID: 24990533     DOI: 10.1002/humu.22613

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  5 in total

1.  Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease.

Authors:  Benjamin Cocanougher; Umut Aypar; Amber McDonald; Linda Hasadsri; Michael J Bennett; W Edward Highsmith; Kristin D'Aco
Journal:  Mol Genet Metab Rep       Date:  2015-01-21

Review 2.  Galactosemia: Towards Pharmacological Chaperones.

Authors:  Samantha Banford; Thomas J McCorvie; Angel L Pey; David J Timson
Journal:  J Pers Med       Date:  2021-02-07

3.  Analysis of the Structure-Function-Dynamics Relationships of GALT Enzyme and of Its Pathogenic Mutant p.Q188R: A Molecular Dynamics Simulation Study in Different Experimental Conditions.

Authors:  Anna Verdino; Gaetano D'Urso; Carmen Tammone; Bernardina Scafuri; Anna Marabotti
Journal:  Molecules       Date:  2021-09-30       Impact factor: 4.411

4.  Investigating the Effects of Amino Acid Variations in Human Menin.

Authors:  Carmen Biancaniello; Antonia D'Argenio; Deborah Giordano; Serena Dotolo; Bernardina Scafuri; Anna Marabotti; Antonio d'Acierno; Roberto Tagliaferri; Angelo Facchiano
Journal:  Molecules       Date:  2022-03-07       Impact factor: 4.411

5.  Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia.

Authors:  Benjamin Cocanougher; Umut Aypar; Amber McDonald; Linda Hasadsri; Michael J Bennett; W Edward Highsmith; Kristin D׳Aco
Journal:  Data Brief       Date:  2015-02-07
  5 in total

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