Article
Molecular basis of classic galactosemia from the structure of human galactose 1-phosphate uridylyltransferase.
Human molecular genetics - 1 Jun 2016
McCorvie Thomas J, Kopec Jolanta, Pey Angel L, Fitzpatrick Fiona, Patel Dipali, Chalk Rod, Shrestha Leela, Yue Wyatt W
Abstract excerpt
Classic galactosemia is a potentially lethal disease caused by the dysfunction of galactose 1-phosphate uridylyltransferase (GALT). Over 300 disease-associated GALT mutations have been reported, with the majority being missense changes, although a better understanding of their underlying molecular effects has been hindered by the lack of structural information for the human enzyme. Here, we present the 1.9 Å...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
