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Parsch, J., Russell, J.A., Beerman, I., Hartl, D.L. and Stephan, W. (2000) Deletion of a conserved regulatory element in the Drosophila Adh gene leads to increased alcohol dehydrogenase activity but also delays development. Genetics, 156(1), 219-227.

has been cited by the following article:

• TITLE: Identification of structurally and functionally significant deleterious nsSNPs of GSS gene: in silico analysis

  AUTHORS: Ramavartheni Kanthappan, Rao Sethumadhavan

  KEYWORDS: GSS Gene; SNP; Glutathione Synthetase; SIFT; PolyPhen; UTRScan

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.1 No.4, October 27, 2010

  ABSTRACT: It is becoming more and more apparent that most genetic disorders are caused by biochemical abnormalities. Recent advances in human genome project and related research have showed us to detect and understand most of the inborn errors of metabolism. These are often caused by point mutations manifested as single-nucleotide-polymorphisms (SNPs). The GSS gene inquested in this work was analyzed for potential mutations with the help of computational tools like SIFT, PolyPhen and UTRscan. It was noted that 84.38% nsSNPs were found to be deleterious by the sequence homology based tool (SIFT), 78.13% by the structure homology based tool (PolyPhen) and 75% by both the SIFT and PolyPhen servers. Two major mutations occurred in the native protein (2HGS) coded by GSS gene at positions R125C and R236Q. Then a modeled structure for the mutant proteins (R125C and R236Q) was proposed and compared with that of the native protein. It was found that the total energy of the mutant (R125C and R236Q) proteins were -31893.846 and -31833.818 Kcal/mol respectively and that of the native protein was -31977.365 Kcal/mol. Also the RMSD values between the native and mutant (R125C and R236Q) type proteins were 1.80Å and 1.54Å. Hence, we conclude based on our study that the above mutations could be the major target mutations in causing the glutathione synthetase deficiency.