Domain relationships in thiamine diphosphate-dependent enzymes


Autoria(s): Duggleby, RG
Data(s)

01/01/2006

Resumo

Three-dimensional structures have been determined for 13 different enzymes that use thiamine diphosphate (ThDP) as a cofactor. These enzymes fall into five families, where members within a family have similar structures. In different families, there are similarities between some domains that clearly point to a common ancestor for all of these enzymes. Where the enzyme structures differ, evolutionary relationships between families can be discerned. Here, I present an analysis of these families and propose an evolutionary pathway to explain the diversity of structures that are now known.

Identificador

http://espace.library.uq.edu.au/view/UQ:79909

Idioma(s)

eng

Publicador

Amer Chemical Soc

Palavras-Chave #Chemistry, Multidisciplinary #Pyruvate-ferredoxin Oxidoreductase #Acetohydroxyacid Synthase #Multienzyme Complex #Angstrom Resolution #Crystal-structures #Active-site #Decarboxylase #Dehydrogenase #Binding #Transketolase #C1 #270108 Enzymes #270208 Molecular Evolution #780105 Biological sciences
Tipo

Journal Article