Literature DB >> 18490185

Structural consequences of amino acid substitutions causing Tay-Sachs disease.

Kazuki Ohno1, Seiji Saito, Kanako Sugawara, Hitoshi Sakuraba.   

Abstract

To determine the structural changes in the alpha-subunit of beta-hexosaminidase due to amino acid substitutions causing Tay-Sachs disease, we built structural models of mutant alpha-subunits resulting from 33 missense mutations (24 infantile and 9 late-onset), and analyzed the influence of each amino acid replacement on the structure by calculating the number of atoms affected and determining the solvent-accessible surface area of the corresponding amino acid residue in the wild-type alpha-subunit. In the infantile Tay-Sachs group, the number of atoms influenced by a mutation was generally larger than that in the late-onset Tay-Sachs group in both the main chain and the side chain, and residues associated with the mutations found in the infantile Tay-Sachs group tended to be less solvent-accessible than those in the late-onset Tay-Sachs group. Furthermore, color imaging determined the distribution and degree of the structural changes caused by representative amino acid substitutions, and that there were also differences between the infantile and late-onset Tay-Sachs disease groups. Structural study is useful for elucidating the basis of Tay-Sachs disease.

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Year:  2008        PMID: 18490185     DOI: 10.1016/j.ymgme.2008.04.006

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  6 in total

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Authors:  Jaqueline A Picache; Wei Zheng; Catherine Z Chen
Journal:  Front Pharmacol       Date:  2022-07-05       Impact factor: 5.988

2.  Structural characterization of mutant alpha-galactosidases causing Fabry disease.

Authors:  Kanako Sugawara; Kazuki Ohno; Seiji Saito; Hitoshi Sakuraba
Journal:  J Hum Genet       Date:  2008-07-17       Impact factor: 3.172

3.  Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India.

Authors:  Mehul Mistri; Sanjeev Mehta; Dhaval Solanki; Mahesh Kamate; Neerja Gupta; Madhulika Kabra; Ratna Puri; Katta Girisha; Sankar Hariharan; Sheela Nampoothiri; Frenny Sheth; Jayesh Sheth
Journal:  J Hum Genet       Date:  2019-08-06       Impact factor: 3.172

4.  Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from India.

Authors:  Mehul Mistri; Parag M Tamhankar; Frenny Sheth; Daksha Sanghavi; Pratima Kondurkar; Swapnil Patil; Susan Idicula-Thomas; Sarita Gupta; Jayesh Sheth
Journal:  PLoS One       Date:  2012-06-18       Impact factor: 3.240

5.  Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.

Authors:  Jayesh Sheth; Mehul Mistri; Chaitanya Datar; Umesh Kalane; Shekhar Patil; Mahesh Kamate; Harshuti Shah; Sheela Nampoothiri; Sarita Gupta; Frenny Sheth
Journal:  Mol Genet Metab Rep       Date:  2014-09-29

6.  Tay-Sachs disease mutations in HEXA target the α chain of hexosaminidase A to endoplasmic reticulum-associated degradation.

Authors:  Devin Dersh; Yuichiro Iwamoto; Yair Argon
Journal:  Mol Biol Cell       Date:  2016-09-28       Impact factor: 4.138

  6 in total

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