Title : Beta conformation of polyglutamine track revealed by a crystal structure of Huntingtin N-terminal region with insertion of three histidine residues.

Pub. Date : 2013 May-Jun

PMID : 23370273






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington disease is an autosomal-dominant neurodegenerative disorder caused by a polyglutamine (polyQ) expansion (> 35Q) in the first exon (EX1) of huntingtin protein (Htt). polyglutamine FERM domain containing 6 Homo sapiens
2 Huntington disease is an autosomal-dominant neurodegenerative disorder caused by a polyglutamine (polyQ) expansion (> 35Q) in the first exon (EX1) of huntingtin protein (Htt). polyglutamine FERM domain containing 6 Homo sapiens